Protocol summary
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Study aim
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Determination of the effect of sildenafil on the clinical manifestations of myocardial ischemia in patients with coronary slow flow
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Design
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Clinical trial with control group, with parallel groups, three-way blind, randomized, phase 2 on 20 patients
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Settings and conduct
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10 patients with slow coronary blood flow in Afshar Hospital in Yazd will be prescribed sildenafil for 3 months and we will study the effects of this drug on improving patients' heart symptoms and changes in their ETT
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Participants/Inclusion and exclusion criteria
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Inclusion criteria:
Definitive diagnosis of CSFP on coronary angiography ;Clinical signs of ischemia include typical angina pectoris or dyspnea.
Exclusion criteria:
Patients with myocardial infarction or PCI or CABG or valve replacement or repair; Patients with Obstructive CAD (stenosis greater than 40%); Patients with hepatic or renal insufficiency or CVA or COPD or Cancer or acute infectious disease such as Covid 19; Patients older than 70 years or less than 30 years; Patients with low systolic blood pressure (less than 90 mmHg); Patients with severe uncontrolled hypertension (more than 180/100); Patients with aneurysm or ectasia or no-reflow or spasm or dissection or systolic heart failure or valvular disease; Patients with LVEF less than 50%
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Intervention groups
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Sildenafil will be prescribed to half of the patients, the treatment will start with a daily dose of 50 mg orally and will continue for 12 weeks.
In the other half of the patients who are in the control group, like the intervention group, placebo medicine is prescribed instead of sildenafil tablets.
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Main outcome variables
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Clinical symptoms,ETT changes,readmission rate
General information
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Reason for update
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Completion of information on the exact date of enrollment and Changing the drug administration method from 25 mg twice a day to 50 mg daily
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Acronym
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IRCT registration information
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IRCT registration number:
IRCT20220223054103N1
Registration date:
2022-04-28, 1401/02/08
Registration timing:
prospective
Last update:
2023-07-11, 1402/04/20
Update count:
1
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Registration date
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2022-04-28, 1401/02/08
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Registrant information
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Recruitment status
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Recruitment complete
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Funding source
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Expected recruitment start date
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2022-06-22, 1401/04/01
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Expected recruitment end date
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2022-10-23, 1401/08/01
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Actual recruitment start date
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2022-06-26, 1401/04/05
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Actual recruitment end date
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2022-09-19, 1401/06/28
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Trial completion date
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2022-12-19, 1401/09/28
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Scientific title
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Effect of Sildenafil on Ischemic Cardiac Clinical and paraclinical manifestations in patients with Coronary Slow Flow Phenomenon : a randomized controlled clinical trial
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Public title
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Effect of Sildenafil on Coronary Slow Flow Phenomenon
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Purpose
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Supportive
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Inclusion/Exclusion criteria
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Inclusion criteria:
Patients with definitive diagnosis of CSFP on coronary angiography.
Patients with clinical signs of ischemia including typical angina pectoris (at least 2-3 minutes retrosternal and compressive angina) or dyspnea (equivalent to angina).
Exclusion criteria:
Patients with myocardial infarction or PCI or CABG or valve replacement or valve repair
Patients with Obstructive CAD (stenoses greater than 40%)
Patients with hepatic or renal failure or CVA or COPD or Cancer or acute infectious disease such as Covid 19
Patients older than 75 years or less than 30 years
Patients with low systolic blood pressure (<90 mmHg)
Patients with severe uncontrolled hypertension (> 180/100)
Patients with LVEF <50%
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Age
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From 30 years old to 70 years old
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Gender
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Both
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Phase
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2-3
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Groups that have been masked
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- Participant
- Care provider
- Investigator
- Outcome assessor
- Data analyser
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Sample size
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Target sample size:
20
Actual sample size reached:
20
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Randomization (investigator's opinion)
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Randomized
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Randomization description
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Randomization will be done based on the quadruple block method.The letters A and B will be used to assign the drug and the placebo. Until the drug is assigned, it will not be clear which A and B belong to the drug or the placebo. Only one person (the main executor) is aware. For concealment, the person who performs the randomization and specifies the following arrangements (AABB ,ABAB, ABBA, BBAA, BABA, BAAB) will be different from the person delivering the drug to the patient.For randomization, random order of 4 is noted and each block is placed in a sealed envelope. After registering all the patients, each patient is given a code. After the blocks are randomized, the randomized sequences are numbered sequentially. The person who allocates the drug assigns the prepared drugs to the patient after opening each envelope.
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Blinding (investigator's opinion)
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Triple blinded
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Blinding description
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A person who is aware of the assignment of the letters A and B to a drug or placebo is only the first executor and project manager. Other people who do randomization and drug allocation and examination and evaluation of patient outcomes and statistical analysis are different people and do not know which letter is assigned to the drug or placebo.The drugs are available to the dispenser in the same form in completely similar packages, and the patient himself is also unaware that he is receiving the drug or placebo. The drug packages are unnamed and are only in boxes A and B. The dispenser and the doctor are not aware of the contents of boxes A and B.
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Placebo
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Used
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Assignment
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Parallel
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Other design features
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Ethics committees
1
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Ethics committee
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Approval date
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2022-04-04, 1401/01/15
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Ethics committee reference number
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ssu.rec.1401.002
Health conditions studied
1
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Description of health condition studied
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Coronary Slow Flow Phenomenon
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ICD-10 code
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I25.118
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ICD-10 code description
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Atherosclerotic heart disease of native coronary artery with other forms of angina pectoris
Primary outcomes
1
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Description
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Chest Pain according to Canadian cardiovascular society classification
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Timepoint
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Begining of the study, 1 , 2 , 3 months after taking sildenafil
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Method of measurement
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Canadian cardiovascular society classification questionnaire
2
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Description
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Duke treadmill score
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Timepoint
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Begining of the study, 3 months after taking sildenafil or placebo
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Method of measurement
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Scoring based on the Duke treadmill score
3
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Description
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Functional capacity in exercise treadmill test
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Timepoint
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Begining of the study, 3 months after taking sildenafil or placebo
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Method of measurement
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Achived METs
Secondary outcomes
1
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Description
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ETT changes
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Timepoint
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begining of the study and 3 months later
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Method of measurement
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exercise treadmill test
2
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Description
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blood pressure
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Timepoint
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begining of the study and 1 and 2 and 3 months later
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Method of measurement
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Blood pressure monitor
Intervention groups
1
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Description
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Intervention group: The use of Sildenafil starts with a daily dose of 50 mg orally and continues for 12 weeks.
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Category
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Treatment - Drugs
2
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Description
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Control group: The placebo is started once daily orally and continues like the intervention group until the end of the study.
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Category
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Placebo
1
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Sponsor
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Grant name
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Grant code / Reference number
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Is the source of funding the same sponsor organization/entity?
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Yes
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Title of funding source
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Yazd University of Medical Sciences
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Proportion provided by this source
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100
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Public or private sector
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Public
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Domestic or foreign origin
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Domestic
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Category of foreign source of funding
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empty
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Country of origin
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Type of organization providing the funding
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Academic
Sharing plan
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Deidentified Individual Participant Data Set (IPD)
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Undecided - It is not yet known if there will be a plan to make this available
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Study Protocol
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Undecided - It is not yet known if there will be a plan to make this available
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Statistical Analysis Plan
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Undecided - It is not yet known if there will be a plan to make this available
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Informed Consent Form
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Undecided - It is not yet known if there will be a plan to make this available
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Clinical Study Report
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Undecided - It is not yet known if there will be a plan to make this available
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Analytic Code
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Not applicable
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Data Dictionary
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Not applicable