- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05043948
Genome-wide Association Study of Development of Collateral Circulation for Patients With Coronary or Peripheral Artery Disease (GWAScollateral)
September 12, 2021 updated by: Jung-min Ahn
The purpose of this study is to evaluate the genome-wide association for the development of collateral circulation for patients with coronary or peripheral artery disease and to develop the molecular genetic treatment model based on genome-wide association data.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
400
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jung-hee Ham, Project manager
- Phone Number: 82230104728
- Email: cvcrc5@amc.seoul.kr
Study Locations
-
-
-
Seoul, Korea, Republic of
- Recruiting
- Asan Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with chronic total coronary or peripheral occlusion
Description
Inclusion Criteria:
- Age more than 20
- Chronic total occlusive lesion from the coronary or peripheral angiogram
Exclusion Criteria:
- Renal dysfunction
- Hepatic dysfunction
- Thrombocythemia or thrombocythemia
- Planned major surgery in 1 year
- History of gastrointestinal haemorrhage
- Malignant tumor
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Coronary Artery Disease_collateral flow grade 2
|
for evaluation of the genome-wide association study
|
|
Coronary Artery Disease_collateral flow grade 0
|
for evaluation of the genome-wide association study
|
|
Peripheral Artery Disease_collateral flow grade 2
|
for evaluation of the genome-wide association study
|
|
Peripheral Artery Disease_collateral flow grade 0
|
for evaluation of the genome-wide association study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Correlation between genome and collateral flow
Time Frame: 5 years
|
5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 21, 2015
Primary Completion (Anticipated)
June 30, 2025
Study Completion (Anticipated)
December 31, 2025
Study Registration Dates
First Submitted
September 12, 2021
First Submitted That Met QC Criteria
September 12, 2021
First Posted (Actual)
September 14, 2021
Study Record Updates
Last Update Posted (Actual)
September 14, 2021
Last Update Submitted That Met QC Criteria
September 12, 2021
Last Verified
September 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GWAS_collateral
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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