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moderate COVID-19 Design: This is a parallel 2-arm randomized, controlled, double-blind, single center (...) will be blinded Participants/Inclusion and exclusion criteria: All mild to moderate COVID-19 infected (...) breastfeeding, any prior experimental treatment for COVID-19, taking Amiodarone and Rifampin, evidence of
IRCTID: IRCT20200328046886N1
clinical and laboratory symptoms in patients with Covid-19: Clinical trial Design: The clinical trial has (...) number assigned to each patient. Settings and conduct: In Razi Hospital, Ahvaz, two groups of Covid-19 (...) confirmation of Covid 19 based on PCR results and approved global health clinical signs confirmed by a
IRCTID: IRCT20200330046897N1
Study aim: Clinical trial of the effects of elderberry extract syrup against COVID-19 symptoms in outpatients and home quarantined patients Design: This is a randomized, double-blinded, placebo controlled (...) quarantined patients. 40 patients with COVID-19 disease will be selected and randomly assigned to two groups
IRCTID: IRCT20200406046965N1
manifestations of patients with probable or confirmed COVID-19 Design: This pilot clinical trial will be performed on 15 hospitalized patients with probable or confirmed COVID-19, as before-after trial without (...) assigned for COVID-19 patients. This research will be carried out in April of 2020. Participants/Inclusion
IRCTID: IRCT20200405046960N1
Study aim: Evaluation the effect of crocetin in improving the clinical and laboratory symptoms of patients with COVID-19 Design: A randomized, blinded, placebo-controlled clinical trial with a parallel (...) study will be performed on outpatients. In this study, 40 patients with COVID-19 disease were selected
IRCTID: IRCT20081019001369N3
Study aim: Comparing safety and efficacy of Favipiravir and Kaletra in COVID-19 Design: In this (...) criteria: Inclusion criteria: Diagnosis of COVID-19 based on either ground glass appearance in chest CT scan or positive RT-PCR test for COVID-19; Requiring hospitalization; Patient's age between 16 and 100
IRCTID: IRCT20150808023559N20
  1. Evaluation of safety and efficacy of hydroxychloroquine plus favipiravir drug regimen in comparison with hydroxychloroquine plus kaletra on the need for intensive care unit treatment in patients with COVID-19; a randomized, multicenter, parallel groups, open label study
  2. Safety and efficacy of “Hydroxychloroquine + Azithromycin + Naproxen + Prednisolone” and “Hydroxychloroquine + Azithromycin + Naproxen” regimens in comparison with “Hydroxychloroquine + kaletra” on the need for intensive care unit treatment in patients with COVID-19; a randomized, multicenter, parallel groups, open label study
  3. Evaluation the efficacy and safety of Favipiravir made by Shahid Beheshti University of Medical Sciences in comparison with Lopinavir-ritonavir in COVID-19 patients
  4. Evaluation of safety and effectiveness of favipiravir in comparison with Tenofovir Alafenamid in hospitalized patients with COVID-19
  5. Efficacy and safety evaluation of therapeutic regimen of lopinavir/ritonavir and interferon beta 1b in patients with COVID-19
  6. Effect of Intravenous immunoglobulin (IVIG) versus Kaletra (lopinavir and ritonavir) tablets in patients with acute respiratory infection (COVID-19): A clinical trial studies
  7. Comparing the effectiveness of Lopinavir/Ritonavir/Hydroxychloroquine and Atazanavir/Ritonavir/Dolutegravir/Hydroxychloroquine treatment regiments in moderate to severe COVID-19 patients
  8. Comparison of the efficacy and safety of Atazanavir/Ritonavir plus Hydroxychloroquine regimen with Lopinavir/Ritonavir plus Hydroxychloroquine regimen in patients with moderate COVID-19, A randomized, double-blind study
  9. Evaluation the efficacy and safety of Umifenovir (Arbidol) Administration in comparison with Lopinavir-ritonavir (Kaletra) in COVID-19 patients
  10. Evaluating efficacy and safety of hydroxychloroquine + lopinavir or atazanavir/ritonavir combination in patients with COVID-19
moderate COVID-19 Design: This is a non-randomized open label, parallel group clinical trial on 60 patients with mild to moderate covid-19 (30 patients in treatment group and 30 patients in control (...) to moderate covid-19 who refer to Sharif Clinic, Mashhad, Iran. They whether will received two
IRCTID: IRCT20200408046990N1
  1. Evaluation of colchicine tablet efficacy as an adjuvant treatment for patients with mild to moderate COVID-19 in Qaem Hospital, Mashhad: A triple-blind randomized placebo controlled clinical trial
  2. Evaluation of melatonin tablet efficacy as an adjuvant treatment for patients with mild to moderate COVID-19 in Qaem and Imam Reza Hospital, Mashhad: A triple-blind randomized placebo controlled clinical trial
  3. Evaluation of atorvastatin tablet efficacy as an adjuvant treatment for patients with mild to moderate COVID-19 in Qaem Hospital, Mashhad: A double-blind randomized placebo controlled clinical trial
  4. The efficacy and safety of Ivermectin in patients with COVID-19: a randomized clinical trial
  5. Evaluating efficacy and safety of sofosbuvir/ ledipasvir in treatment of COVID-19
  6. Effects of Viroherb capsule and Fenugreek syrup derived from traditional Persian medicine on clinical and paraclinical outcomes and survival of patients with mild to moderate COVID-19 hospitalized in medical centers of Tehran University of Medical Sciences
  7. A single-arm multicenter clinical trial to evaluate the safety and efficacy of Remdesivir in COVID-19 patients with progressive severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
  8. Prognostic Efficacy of Moderate Intensity rosuvastatin on the Infected cases with SARS-Cov-2
  9. Evaluation of the efficacy of oral curcumin on recurrency and number of complex aphthous lesions in the patients referred to the Oral and maxillofacial medicine Department of Guilan Dental School in 2021-2022
  10. The evaluation of safety and efficacy of Favipiravir (ABIDI Pharmaceutical Co, Iran) to shorten the contagiousness in patients with mild to moderate COVID-19
: Laboratory confirmed COVID-19 with RT-PCR, Age over 18 years old, Oxygen saturation < 93%, Fever more than 72 (...) of COVID-19 Critical phase of COVID-19 and Pancreatitis Intervention groups: In this study, patients (...) Study aim: Evaluation the efficacy and safety of Sitagliptin administration in patients with COVID
IRCTID: IRCT20200420047147N1
  1. Evaluation the efficacy and safety of Favipiravir made by Shahid Beheshti University of Medical Sciences in comparison with Lopinavir-ritonavir in COVID-19 patients
  2. Evaluation the efficacy and safety of Umifenovir (Arbidol) Administration in comparison with Lopinavir-ritonavir (Kaletra) in COVID-19 patients
  3. Evaluation the Efficacy and Safety of Tocilizumab in Patients with Novel Coronavirus (COVID-19)
  4. Evaluting the therapeutic and adverse effects of Interferon beta 1-a subcutaneous administration in patients with novel Coronavirus (COVID-19)
  5. The effect of pentaglobin in the treatment of critically ill patients with COVID-19
  6. Evaluating efficacy and safety of hydroxychloroquine + lopinavir or atazanavir/ritonavir combination in patients with COVID-19
  7. Evaluation of safety and efficacy of hydroxychloroquine plus favipiravir drug regimen in comparison with hydroxychloroquine plus kaletra in hospitalized patients with COVID-19
  8. Evaluation of safety and efficacy of hydroxychloroquine plus favipiravir drug regimen in comparison with hydroxychloroquine plus kaletra on the need for intensive care unit treatment in patients with COVID-19; a randomized, multicenter, parallel groups, open label study
  9. Safety and efficacy of “Hydroxychloroquine + Azithromycin + Naproxen + Prednisolone” and “Hydroxychloroquine + Azithromycin + Naproxen” regimens in comparison with “Hydroxychloroquine + kaletra” on the need for intensive care unit treatment in patients with COVID-19; a randomized, multicenter, parallel groups, open label study
  10. Efficacy and safety evaluation of therapeutic regimen of lopinavir/ritonavir and interferon beta 1b in patients with COVID-19
forms of covid-19 virus Design: Randomized controlled trial study; double-blind; parallel groups; on (...) symptoms of covid-19 disease Do not have positive test Intervention groups: Intervention Group is500 (...) outcome variables: - COVID-19 Mild type (fever - cough - shortness of breath and positive PCR test
IRCTID: IRCT20200421047153N1
  1. A Field Trial to examine the effect of hydroxychloroquine prophylaxis in preventing the sever forms of COVID-19 infection in asymptomatic healthcare workers (A double blind placebo controlled study)
  2. Evaluation of treatment strategy Included : hydroxychloroquine ,naproxen and oseltamivir for outpatient patients with Covid 19
  3. Evaluate the efficacy of hydroxychloroquine in the prevention of SARS-COV2 infection in high risk health care workers
  4. The prophylactic effect of oral hydroxy-chloroquine in close contacts of COVID-19 patients
  5. Evaluation of the efficiency of hydroxychloroquine drug regimen in comparison with hydroxychloroquine + azithromycin in hospitalized patients with covid-19 in the intensive care unit
  6. Evaluation of the efficacy of N-Acetylcysteine in severe COVID-19 patients: a randomized controlled phase III clinical trial
  7. The effect of vitamin C and E in the treatment and clinical course of patients with SARS-cov2 (COVID-19)
  8. Evaluation the efficacy and safety of Hydroxychloroquine administration for COVID-19 post exposure prophylaxis
  9. Evaluation of efficacy of pharmacotherapy treatment of COVID- 19 infection using oral Levamisole and Formoterol+Budesonide inhaler and comparison of this treatment protocol with standard national treatment of the disease
  10. Evaluation of safety and efficacy of hydroxychloroquine plus favipiravir drug regimen in comparison with hydroxychloroquine plus kaletra on the need for intensive care unit treatment in patients with COVID-19; a randomized, multicenter, parallel groups, open label study
Study aim: Determination of the grapefruit seed extract efficacy in the treatment of COVID-19 as an (...) volunteer patients with COVID-19 at Masih Daneshvari Hospital in Tehran confirmed by PCR. Patients (...) above 18 and under 60 years old, that their COVID-19 is confirmed by PCR test, and don't have any
IRCTID: IRCT20140312016968N2
COVID-19 Design: This is a randomized triple-blind, parallel group clinical trial on 40 patients with mild to moderate covid-19 (20 patients in treatment group and 20 patients in placebo group). Settings (...) moderate covid-19 who refer to Quem Hospital, Mashhad, Iran. They whether will received one colchicine 1mg
IRCTID: IRCT20200408046990N2
Study aim: Investigating the efficacy and safety of Nivasha oral spray in controlling the symptoms of patients with COVID-19 Design: This study is a multi-center, prospective, randomized, open (...) cough, shortness of breath, fever) confirm COVID-19. Confirmed diagnosis of COVID-19, with RT-PCR
IRCTID: IRCT20080901001165N59
Study aim: A- Finding effective and available treatment for COVID-19 patients B- Comparison of our (...) double blind clinical trial Settings and conduct: Hospitalized COVID-19 positive patients will be (...) and exclusion criteria: All of the COVID-19 hospitalized patients with positive PCR and Chest CT-scan
IRCTID: IRCT20200324046852N1
  1. Evaluation of safety and efficacy of hydroxychloroquine plus favipiravir drug regimen in comparison with hydroxychloroquine plus kaletra on the need for intensive care unit treatment in patients with COVID-19; a randomized, multicenter, parallel groups, open label study
  2. Evaluation of safety and efficacy of hydroxychloroquine plus favipiravir drug regimen in comparison with hydroxychloroquine plus kaletra in hospitalized patients with COVID-19
  3. Evaluation of the effect of Arbidol drug in the treatment of hospitalized patients with COVID-19
  4. The efficacy of inhaled formoterol on symptom improvement in covid 19 patients
  5. Evaluation of Atazanavir/Ritonavir effect on COViD-19 patients treatment in comparison with Lopinavir / Ritonavir
  6. The Efficacy of standard treatment and dimethyl fumarate in the treatment of patients with COVID-19
  7. Effect of Intravenous immunoglobulin (IVIG) versus Kaletra (lopinavir and ritonavir) tablets in patients with acute respiratory infection (COVID-19): A clinical trial studies
  8. Study of Tocilizumab effect on treatment and clinical symptoms and laboratory signs of Iranian COVID-19 patients: a ‎crinical trial study
  9. Safety and efficacy of “Hydroxychloroquine + Azithromycin + Naproxen + Prednisolone” and “Hydroxychloroquine + Azithromycin + Naproxen” regimens in comparison with “Hydroxychloroquine + kaletra” on the need for intensive care unit treatment in patients with COVID-19; a randomized, multicenter, parallel groups, open label study
  10. The effect of naproxen on the healing process of patients with COVID-19
coronavirus pneumonia (COVID-19) Design: A randomized controlled clinical trial with parallel groups (...) Department of Health for Covid-19, are a quarantine candidate and receive home treatment. Participants/Inclusion and exclusion criteria: patients with 18-65 years old, developing mild to moderate COVID-19 based
IRCTID: IRCT20180923041093N4
covid-19 Design: Phase 3,2 arms each arms 50 patients, block randomization Two arm parallel group (...) criteria: Inclusion criteria: -age>18 -Patients with probable and definitive diagnosis of covid-19 (...) or imaging findings for covid-19 Exclusion criteria: -Patients or companion dissatisfaction to enter
IRCTID: IRCT20200322046833N1
  1. Evaluation the efficacy and safety of Umifenovir (Arbidol) Administration in comparison with Lopinavir-ritonavir (Kaletra) in COVID-19 patients
  2. Evaluation of efficacy and safety of adding Chlorpromazine to Atazanavir/Ritonavir regimen in the treatment of COVID-19 patients, a randomized double-blind clinical trial
  3. Comparison of the efficacy and safety of Atazanavir/Ritonavir plus Hydroxychloroquine regimen with Lopinavir/Ritonavir plus Hydroxychloroquine regimen in patients with moderate COVID-19, A randomized, double-blind study
  4. Safety and Effectiveness of azithromycin in Patients with COVID-19 Referred to zeiaeian Hospital : A clinical trial study
  5. Comparing the effectiveness of Lopinavir/Ritonavir/Hydroxychloroquine and Atazanavir/Ritonavir/Dolutegravir/Hydroxychloroquine treatment regiments in moderate to severe COVID-19 patients
  6. evaluation of the effects of the 2-drug diet (hydroxychloroquine + umifenovir(Arbidol)) compared with Hydroxy chlorquine on the of mortality rate in patients with moderate symptoms of COVID-19 infections: A randomized interventional study in Imam Reza Hospital, Mashhad.
  7. Investigating the efficacy and safety of Umifenovir in controlling the symptoms of patients with COVID-19
  8. Evaluating efficacy and safety of hydroxychloroquine + lopinavir or atazanavir/ritonavir combination in patients with COVID-19
  9. Evaluating effectiveness and safety of Umifenovir in the treatment (COVID-19)infection In patients referred to Tehran Imam Khomeini Hospital Complex
  10. Evaluation of effectiveness‎ of Intravenous vitamin c in Patients with COVID-19 Referred to Imam ‎Khomeini Hospital: a clinical trial ‎
Study aim: Evaluation the effect of lithium carbonate in covid-19 patients Design: A randomized, blinded, placebo controlled clinical trial with a parallel group design of 40 patients, randomizing with (...) this study, 40 patients with covid-19 disease were selected and randomly assigned to two groups of 20
IRCTID: IRCT20081019001369N5
patients with COVID-19 infection Design: The study is a non-randomized, single-blind clinical trial (...) university Tehran Medical Sciences on hospitalized COVID-19 patients. Patients are treated in intervention (...) and exclusion criteria: Inclusion criteria: Older than 18 years old, Hospitalized with COVID-19
IRCTID: IRCT20200413047062N1
respiratory failure as well as organs failure and death of COVID-19 disease. Design: Clinical trial with parallel control group , randomisation by balanced block method, phase 2 on 60 COVID-19 patients Settings and conduct: 60 COVID-19 patients admitted to Tabriz Imam Reza Hospital will be divided in 2
IRCTID: IRCT20200406046968N3
the control group will receive the hospital's standard protocol for the treatment of COVID-19. The (...) diagnosed with COVID-19 using the RT-PCR test - having a breathing rate> 30 per minute - Arterial blood (...) burden associated with ARDS, mortality, and the need for hospitalization in patients diagnosed with COVID
IRCTID: IRCT20190418043307N1
micrograms/Kg once every other day for 3 doses plus the usual national protocol of treatment for COVID-19 (...) analyzed using SPSS software. Settings and conduct: In this study, 25 patients with COVID 19 being (...) criteria: 50 patients with COVID 19 disease with no exclusion criteria Exclusion criteria: history of
IRCTID: IRCT20200818048444N3
covid-19 who referred to Booali Hospital in Tehran in 2023 Design: The clinical trial, with parallel (...) criteria: All those who have been infected with Covid-19 for more than 6 months Noticeable hair loss Age 20 (...) treatment of hair loss patients with a history of covid-19
IRCTID: IRCT20230531058350N1
  1. Comparative evaluation of PRP (Platelet-Rich Plasma) with nutritional supplements in improvement of hair loss (telogen effluvium) in patients recovered from COVID-19 in Bam Pasteur hospital in 2022
  2. Comparison of the effectiveness of SLN containing finasteride and finasteride tablets in androgenic alopecia
  3. The effect of supplementation with iron alone and combined with the docosahexaenoic acid and changes in serum lipid profile on risk of Coronary- heart disease via measuring paraoxonase 1, hs-CRP and the ApoB / ApoA1 ratio in women with iron deficiency anemia
  4. The effect of supplementation with iron alone and combined with the docosahexaenoic acid on iron deficiency anemia index and oxidative stress in women with iron deficiency anemia
  5. The effect of oral zinc on nutritional and inflammatory factors in chronic hemodialysis patients
  6. The effect of zinc supplementation on CD4+ lymphocyte cell count in HIV patients in Iranian research center: a randomized double blind controlled trial
  7. The effect of Biotin and Dexpanthenol on hair loss in patients with androgenetic alopecia
  8. Comparing the Effectiveness of Combined Treatment of Carboxy Therapy, Platelet-Rich Plasma (PRP) and Topical Finasteride with Platelet-Rich Plasma Plus Topical Finasteride, in the Treatment of Male Pattern Androgenic Hair Loss
  9. Comparative efficacy study of topical finasteride and topical minoxidil versus topical minoxidil alone in male patients with androgenic alopecia.
  10. Effect of topical finasteride on treatment of patients with androgenic alopecia
with covid-19 (Coronavirus 19 disease) Design: This clinical trial has control group, and with (...) exclusion criteria: Inclusion criteria: Male or female patients 18 years old and older with COVID-19, positive coronavirus 19 PCR, Ground glass view at low-dose CT scan, Arterial oxygen saturation less than 93
IRCTID: IRCT20160131026298N3
Study aim: Determining the effect of eye movements desensitization and reprocessing in real and virtual methods and comparing them on fear of COVID 19 in nurses Design: Controlled clinical trial, with (...) (eye movements desensitization and reprocessing) on fear of covid 19
IRCTID: IRCT20220222054101N1
  1. Comparison of the Effectiveness of compassion therapy and eye movement desensitization and reprocessing therapy (EMDR) on coronary anxiety, uncertainty intolerance, catastrophizing and coping efficiency of patients with coronavirus (COVID-19)
  2. The Effect of Eye Movements Desensitization and Reprocessing on Guilt Feeling , Depression of Parents of Children with Autism Disorder
  3. Evaluation of the effect of desensitization with eye movements and reprocessing on anxiety, hemodynamic parameters and duration of hospitalization in patients with COVID-19
  4. Effectiveness of eye movement desensitization and reprocessing (EMDR) on sexual function of patients with vaginismus
  5. The effect of eye movement desensitization and reprocessing therapy on cognitive failure in nurses working in COVID-19 wards
  6. Investigating the effect of eye movement desensitization and reprocessing (EMDR) on fear of normal vaginal delivery in primiparous women
  7. comparison between the effect of eye movement desensitization and reprocessing (EMDR) and guided imagery on the severity of insomnia and pain of rheumatoid arthritis patients
  8. The effect of Eye Movement Desensitization and Reprocessing (EMDR) on kinesiophobia and ADL in elderly with musculoskeletal pain referring to outpatient clinicin Rafsanjan city in 2023.
  9. Comparison of the Effectiveness of Virtual Reality Exposure Therapy with Eye Movement Desensitization and Reprocessing Therapy on Symptoms of Acrophobia and Anxiety Sensitivity in Adolescent Girls
  10. Comparison of effect of Stress Management, Emotion Regulation, Eye Movement Desensitization and Reprocessing Therapy in Improving Resilience, Repetitive Negative Thoughts, Anxiety and Depression in Patients with Covid 19
Study aim: Evaluation of thrombolytic and anticoagulant in treatment of COVID-19 patients Design: This study is a randomized control trial with tree arm parallel group without double blind. We have (...) : Critical COVID patients with d.Dimer more than 3000 ng/ml Intervention groups: The patients will started
IRCTID: IRCT20200515047456N1
  1. Evaluation of safety and efficacy of intavitreal injection of recombinant Tissue Plasminogen Activator before vitrectomy for diabetic Tractional Retinal Detachment on facility and outcome of surgery
  2. A prospective randomized controlled trial to compare recombinant tissue-type plasminogen activator (rt-PA) and standard treatmentin in patients with ARDS induced by COVID-19
  3. Comparition of Flaxseed and Evening primrose oil with vitamin E on Cyclic Mastalgia in women
  4. Visual acuity and central macular thickness in the hemorrhagic choroid neo-vascularization due to age-related macular degeneration with intravitreal Avastin injection compared with intravitreal injection of tissue plasminogen activator with avastin
  5. The Study of the efficacy, safety and tolerability of low molecular weight heparin vs. unfractionated heparin in patients with embolic stroke due to atrial fibrillation
  6. A comparative study of the effects of tissue plasminogen activator and dual antiplatelet therapy on improvement of the score of the National Institutes of Health Stroke Scale in acute ischemic stroke treatment
  7. Comparition the impact of intraarticular Steroid and intraarticular ozon on improving the symptoms of osteoarthritis of knee
  8. Comparition effect of transcutaneous electrical nerve stimulation and epidural analgesia with lidocaine 1% on pain and prognosis of labour
  9. Effect of Gundelia tournefortii extracts on Plasminogen Activator Inhibitor-1, Thromboxane B2, Lipid Profile, Antioxidant Capacity in Patients with Coronary Artery Disease
  10. Catheter directed thrombolysis versus anticoagulation only in patients with Intermediate-high risk pulmonary emboli-A randomized clinical trial
treatment of prolonged anosmia and hyposmia in patients with Covid-19 Design: Clinical trial without (...) and 60 years Loss of sense of smell after Covid-19 (anosmia or hyposmia that has not improved for more (...) prolonged diminished or loss of sense of smell after Covid 19 disease receive four sessions of TDCS
IRCTID: IRCT20180205038619N2
  1. The effects of addition of transcranial direct current stimulation to therapeutic exercise on pain, functional disability and grip strength in patients with tennis elbow
  2. Whole-Body Cryotherapy (WBC) for COVID-19 recovered patients having anosmia or severe hyposmia
  3. The Effect of Transcranial Direct Current Stimulation on Balance in People with Parkinson’s Disease
  4. Comparison of synergestic effectiveness between cognitive behavioral therapy (CBT) and repeated transcranial magnetic stimulation (rTMS) and transcranial direct current stimulation (tDCS) in cognitive flexibility, attention control, working memory and reducing signs and symptoms of MDD patients
  5. Comparing the Effect of Transcranial Direct Current Stimulation (tDCS) With Cognitive-Behavioral therapy (CBT) Interventions on the stress and anxiety and depression and relapse in abstinent methamphetamine-dependent subjects in Farabi Hospital.
  6. The effects of Transcranial direct current stimulation (tDCS) on balance function in adults with peripheral vertigo
  7. The effectiveness of transcranial Direct Current Stimulation of the brain (tDCS) among people with Depressive Disorder
  8. Effects of Transcranial Direct Current Stimulation (tDCS) on Clinical Symptoms and Neurocognitive Function in Males with Chronic Ankle Instability (CAI)
  9. Effect of bihemispheric transcranial direct current stimulation on the verbal function of patients with post-stroke Broca's aphasia during the subacute phase
  10. Evaluation of the effects of transcranial direct current stimulation on geriatric depression
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