- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04855500
A Single Center Registry of Coronary OCT
April 19, 2021 updated by: Liao Wang, Hainan People's Hospital
A Registry of Coronary Artery Optical Coherence Tomography of Hainan General Hospital
This registry started January 1,2020 to collect patients who recieve coronary OCT imaging in Hainan General Hospital.All enrolled patients will receive 1 year followed-up.
Study Overview
Status
Recruiting
Detailed Description
This registry started January 1,2020.Patients >= 18 years old who recieve coronary OCT imaging in Hainan General Hospital are included in current registry.
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Hainan
-
Haikou, Hainan, China, 570311
- Recruiting
- Hainan General Hospital
-
Contact:
- Wang Liao, MD
- Phone Number: 8613518827831
- Email: crain_lw@163.com
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Subjects who recieved intracoronary OCT imaging during cardiac catheterization are eligible for this registry.
Description
Inclusion Criteria:
- Subjects who recieved intracoronary OCT imaging during cardiac catheterization are eligible for this registry.
Exclusion Criteria:
- None
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Major adverse cardiac events (MACE)
Time Frame: 1 years
|
1 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)
January 1, 2020
Primary Completion (Anticipated)
December 31, 2022
Study Completion (Anticipated)
January 31, 2023
Study Registration Dates
First Submitted
April 19, 2021
First Submitted That Met QC Criteria
April 19, 2021
First Posted (Actual)
April 22, 2021
Study Record Updates
Last Update Posted (Actual)
April 22, 2021
Last Update Submitted That Met QC Criteria
April 19, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- WangLiao002
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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