View older revisions Content changed at 2023-07-11, 1402/04/20

Protocol summary

Study aim
Determination of the effect of sildenafil on the clinical manifestations of myocardial ischemia in patients with coronary slow flow
Design
Clinical trial with control group, with parallel groups, three-way blind, randomized, phase 2 on 20 patients
Settings and conduct
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
Participants/Inclusion and exclusion criteria
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%
Intervention groups
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.
Main outcome variables
Clinical symptoms,ETT changes,readmission rate

General information

Reason for update
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
Acronym
IRCT registration information
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
Registration date
2022-04-28, 1401/02/08
Registrant information
Name
Amin Entezari
Name of organization / entity
Country
Iran (Islamic Republic of)
Phone
+98 35 3834 7651
Email address
aminentezari.2013@gmail.com
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2022-06-22, 1401/04/01
Expected recruitment end date
2022-10-23, 1401/08/01
Actual recruitment start date
2022-06-26, 1401/04/05
Actual recruitment end date
2022-09-19, 1401/06/28
Trial completion date
2022-12-19, 1401/09/28
Scientific title
Effect of Sildenafil on Ischemic Cardiac Clinical and paraclinical manifestations in patients with Coronary Slow Flow Phenomenon : a randomized controlled clinical trial
Public title
Effect of Sildenafil on Coronary Slow Flow Phenomenon
Purpose
Supportive
Inclusion/Exclusion criteria
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%
Age
From 30 years old to 70 years old
Gender
Both
Phase
2-3
Groups that have been masked
  • Participant
  • Care provider
  • Investigator
  • Outcome assessor
  • Data analyser
Sample size
Target sample size: 20
Actual sample size reached: 20
Randomization (investigator's opinion)
Randomized
Randomization description
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.
Blinding (investigator's opinion)
Triple blinded
Blinding description
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.
Placebo
Used
Assignment
Parallel
Other design features

Secondary Ids

empty

Ethics committees

1

Ethics committee
Name of ethics committee
Ethics Committee of Shahid Sadoughi University of Medical Sciences, Yazd
Street address
Shahid Sadoughi Blvd
City
Yazd
Province
Yazd
Postal code
۸۹۱۶۹۷۸۴۷۷
Approval date
2022-04-04, 1401/01/15
Ethics committee reference number
ssu.rec.1401.002

Health conditions studied

1

Description of health condition studied
Coronary Slow Flow Phenomenon
ICD-10 code
I25.118
ICD-10 code description
Atherosclerotic heart disease of native coronary artery with other forms of angina pectoris

Primary outcomes

1

Description
Chest Pain according to Canadian cardiovascular society classification
Timepoint
Begining of the study, 1 , 2 , 3 months after taking sildenafil
Method of measurement
Canadian cardiovascular society classification questionnaire

2

Description
Duke treadmill score
Timepoint
Begining of the study, 3 months after taking sildenafil or placebo
Method of measurement
Scoring based on the Duke treadmill score

3

Description
Functional capacity in exercise treadmill test
Timepoint
Begining of the study, 3 months after taking sildenafil or placebo
Method of measurement
Achived METs

Secondary outcomes

1

Description
ETT changes
Timepoint
begining of the study and 3 months later
Method of measurement
exercise treadmill test

2

Description
blood pressure
Timepoint
begining of the study and 1 and 2 and 3 months later
Method of measurement
Blood pressure monitor

Intervention groups

1

Description
Intervention group: The use of Sildenafil starts with a daily dose of 50 mg orally and continues for 12 weeks.
Category
Treatment - Drugs

2

Description
Control group: The placebo is started once daily orally and continues like the intervention group until the end of the study.
Category
Placebo

Recruitment centers

1

Recruitment center
Name of recruitment center
Afshar Hospital
Full name of responsible person
Amin Entezari
Street address
Afshar Hospital , Jomhuri Blvd
City
Yazd
Province
Yazd
Postal code
۸۹۱۷۹۴۵۵۵۶
Phone
+98 35 3525 5016
Email
yazdheartcenter@gmail.com

Sponsors / Funding sources

1

Sponsor
Name of organization / entity
Yazd University of Medical Sciences
Full name of responsible person
Dr Amirhooshang Mehrparvar
Street address
Shahid Sadoughi Blvd
City
Yazd
Province
Yazd
Postal code
۸۹۱۶۹۷۸۴۷۷
Phone
+98 35 3726 3733
Email
yazdheartcenter@gmail.com
Grant name
Grant code / Reference number
Is the source of funding the same sponsor organization/entity?
Yes
Title of funding source
Yazd University of Medical Sciences
Proportion provided by this source
100
Public or private sector
Public
Domestic or foreign origin
Domestic
Category of foreign source of funding
empty
Country of origin
Type of organization providing the funding
Academic

Person responsible for general inquiries

Contact
Name of organization / entity
Yazd University of Medical Sciences
Full name of responsible person
Amin Entezari
Position
M.D, Specialist
Latest degree
Specialist
Other areas of specialty/work
Cardiology
Street address
Jomhuri Blvd
City
Yazd
Province
Yazd
Postal code
۸۹۱۷۹۴۵۵۵۶
Phone
+98 35 3523 1420
Fax
Email
aminentezari.2013@gmail.com

Person responsible for scientific inquiries

Contact
Name of organization / entity
Yazd University of Medical Sciences
Full name of responsible person
Abas Andishmand
Position
M.D, Specialist
Latest degree
Specialist
Other areas of specialty/work
Cardiology
Street address
Jomhuri Blvd
City
Yazd
Province
Yazd
Postal code
۸۹۱۷۹۴۵۵۵۶
Phone
+98 35 3523 1420
Fax
Email
drandishmand@yahoo.com

Person responsible for updating data

Contact
Name of organization / entity
Yazd University of Medical Sciences
Full name of responsible person
Amin Entezari
Position
M.D, Specialist
Latest degree
Specialist
Other areas of specialty/work
Cardiology
Street address
Jomhuri Blvd
City
Yazd
Province
Yazd
Postal code
۸۹۱۷۹۴۵۵۵۶
Phone
+98 35 3523 1420
Fax
Email
aminentezari.2013@gmail.com

Sharing plan

Deidentified Individual Participant Data Set (IPD)
Undecided - It is not yet known if there will be a plan to make this available
Study Protocol
Undecided - It is not yet known if there will be a plan to make this available
Statistical Analysis Plan
Undecided - It is not yet known if there will be a plan to make this available
Informed Consent Form
Undecided - It is not yet known if there will be a plan to make this available
Clinical Study Report
Undecided - It is not yet known if there will be a plan to make this available
Analytic Code
Not applicable
Data Dictionary
Not applicable
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