- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01647568
Safety of Continuing Anti-platelet Agents During Colonoscopic Polypectomy: A Prospective Study
At our VA hospital, in general, it is the policy of our GI lab to not stop our patients anti-platelet therapy whenever they see us for a routine colonoscopy. We do this because we believe the risk of stopping these sort of medications outweigh the risks of a complication from a colonoscopy.
Therefore, we are enrolling patients who are either on clopidogrel or prasugrel or not on any anti-platelet/anti-coagulant therapy that come to our GI lab routine colonoscopies. We perform the procedure just like we normally would and then follow-up with the patient 7 and 30 days after their procedure.
Study Overview
Status
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Texas
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Dallas, Texas, United States, 75216
- Dallas VA Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients presenting to the GI lab for elective colonoscopy
Exclusion Criteria:
- Patients on Coumadin or other anti-coagulants
- Patients with Inflammatory Bowel Disease
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Control
Patients who are not on any anti-platelet/anti-coagulant therapy and present to our lab for a elective colonoscopy.
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Thienopyridine Users
Patients on Clopidogrel or prasugrel when they present for an elective colonoscopy.
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- DVAMC-09-084
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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