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Study aim:
To determining the effect of combined curcuma herbal distillate on clinical course and laboratory parameters in outpatients with COVID-19
Design:
The controlled clinical trial, with two parallel (...) /Inclusion and exclusion criteria:
Inclusion Criteria:People with COVID-19 with a positive specificity test
, neuromuscular diseases, heart disease
Intervention groups:
The intervention group includes patients with covid-19 who receive respiratory rehabilitation intervention in the rehabilitation center.
The comparison group includes patients with covid-19 who receive remote respiratory rehabilitation intervention.
Main
Study aim:
The effect of natural medicine product (MOCOZIFT®) on clinical manifestations and para clinical features in patients with COVID-19: a randomized clinical trial
Design:
Forth phase of a (...) criteria:
Inclusion criteria: age older than 18 years, patients with COVID-19, prescription of Remdesivir
Study aim:
Determining the effectiveness of albumin administration on attenuation, lung involvement and blood oxygen in patients with covid-19 hospitalized in the intensive care unit with an albumin (...) patients with covid-19 hospitalized in the special care department referring to Shahid Madani Hospital
Study aim:
Determining the effect of progressive muscle relaxation technique on anxiety and sleep quality in patients with Covid-19
Design:
Use blocking method for randomization
Create 6 blocks of 4 such (...) exclusion criteria:
Entry requirements:
1. Confirmation of Covid-19 infection through laboratory findings
the level of daily activities of patients with Covid19
Design:
The present study is a parallel (...)Covid19.
Settings and conduct:
The present study is a parallel randomized two-group clinical trial study that will be performed with the participation of 100 patients with Covid19 in Shahid Beheshti
Study aim:
Determining the effect of Covid-19 self-care education through virtual social networks on quality of life and anxiety in cancer patients
Design:
Clinical trial with control group, with (...) patients
Intervention groups:
In this study, the intervention group of Covid-19 self-care training through
, studies only showed that prone positioning is feasible and effective for COVID-19 patients. so the aim of (...) -intubated COVID-19 patients at HAYATABAD MEDICAL COMPLEX, PESHAWAR.
Design:
Randomized controlled trial
(HFNC) in comparison with non-invasive ventilation (NIV) in patients with COVID-19
Design:
The present (...) trial in patients with covid-19 referred to the corona ward of Masih Daneshvari Hospital in Tehran who (...)
Intervention groups:
Patients with COVID-19 disease who require hospitalization and respiratory support are
preventive behaviors of Covid-19 (handwashing, vaccination, and wearing a mask) in Yazd students
Design:
A (...) change
Changing social environment
Initiation of preventive behaviors from covid-19
Maintaining preventive behavior from covid-19
Study aim:
The effect of cinnora supplement therapy in patients with severe form of COVID-19
Design:
Clinical trial with control group, parallel, and randomized groups on 80 patients. Random number (...) definitive diagnosis of COVID-19, and patients over 18 years.
Exclusion criteria: Patient underwent tumor
Study aim:
Determining the effect of targeted oxygen therapy on the recovery outcomes of Covid-19 patients
Design:
Clinical trial with control and intervention group, randomization, phase3 on 80 patients (...) conduct:
After a visit to the emergency medicine physician and confirmation of COVID-19 by physician
Study aim:
Comparison of the effect of vitamin C and N-acetyl cysteine (NAC) on improving clinical symptoms and reducing the duration of hospitalization in patients with covid-19
Design:
The study will be (...) parallel. The trial phase will be 3
Settings and conduct:
Patients with covid-19 in Arak are divided into
Study aim:
The aim of this study was to evaluate the effect of high dose intravenous vitamin C in COVID-19 patients admitted to the intensive care unit.
Design:
Clinical trial with control group, with (...) from the study.
Intervention groups:
Intervention group: COVID-19 patients will receive standard drugs
Study aim:
The effect of laser therapy on pulmonary function and inflammatory factors in patients with Covid19 in the acute phase of the disease
Design:
َA randomized controlled double-blind clinical (...) .
Participants/Inclusion and exclusion criteria:
Inclusion criteria included individuals with COVID-19 with a
diagnosis of COVID-19, which subsequently develops acute respiratory distress syndrome (mild or moderate). COVID-19 patients with severe underlying disease or allergies to the ٍExosomes or its associated
Study aim:
Verifying the effect of the bromhexine hydrochloride on the COVID19 disease compared to placebo
Design:
Two patient groups receiving either the Bromhexine hydrochloride 8 mg or placebo every 8 hours for 16 days
Settings and conduct:
EmamReza Hospital
Participants/Inclusion and exclusion criteria:
COVID19 patients diagnoses according to three diagnostic criteria of this protocol and are 18 year of age or older
Intervention groups:
Two patient groups receiving either the Bromhexine hydrochloride 8 mg or placebo every 8 hours for 16 days
Main outcome variables:
ICU transfer, Intubation and Mechanical Ventilation, Survival/Mortality
Study aim:
Investigating the effect of oral supplementation containing jujube and saffron on recovery and controlling the symptoms of patients with covid-19
Design:
A clinical trial with control (...) paraclinical confirmation of Covid-19; Absence of underlying disease including diabetes, thyroid disorders
have a COVID19-positive PCR, or a CT scan that meets COVID19 criteria, or both enter the (...) Study aim:
Determining the effects of melatonin in improving the condition of patients with COVID19
Design:
This study was performed on 100 COVID19 hospitalized patients .
Randomization block
Study aim:
The aim of this study is to evaluate the effect of balloon-blowing on dyspnea and oxygenation in non-critical Covid-19 patients.
Design:
A clinical trial with a control group, one-way blind (...) criteria:
Inclusion criteria: ≥ 18 years old; Patients with a definitive diagnosis of Covid-19
Study aim:
Evaluation of the effect of Propolis in the treatment of COVID19 patients
Design:
This clinical trial was performed on 72 patients, divided into two groups of 36, including a control group and (...)Covid-19 National Guidelines. Patients in the intervention group, in addition to the standard treatment
(COVID-19) in Weak to Moderate Stages.
Design:
100 patients who will be randomly assigned to two groups (...) Ganjavian hospital who will be diagnosed by the physician at the initial visit of COVID-19 and volunteer to (...) drug. 100 (men and women of different ages) from patients with COVID-19, referred to Ganjuyan Hospital
Study aim:
Evaluation of the effect of Afsantin in the treatment of COVID19 patients
Design:
This clinical trial was performed on 80 patients, divided into two groups of 40, including a control group and (...) groups:
Patients in both groups receive the treatment based on the Covid-19 National Guidelines. Patients
Study aim:
Determining the Effectiveness of L-carnitine Supplementation on Clinical Outcomes in Hospitalized COVID-19 Patients
Design:
This clinical trial has two intervention and control groups, which are (...) groups:
Patients in both intervention and control groups are routinely treated for COVID-19 according to