Colonoscopy Clinical Trials

Clinical trials related to Colonoscopy Procedure

Aspirin Continuation or Interruption in Patients at Moderate Risk for Cardiovascular Events Undergoing Colonoscopy and/or Polypectomy; a Placebo-controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

One in 4 adults between 50 and 80 reports taking regular aspirin. The prevalence of aspirin uses increases with age as well as co-morbid vascular diseases. Patients with cardiovascular diseases are at risk of developing colorectal neoplasms. In patients undergoing screening colonoscopy, interruption of aspirin is believed to be associated with increased cardiovascular events. Continuation of aspirin can however be associated with an increased risk of post-polypectomy bleeding. International guidelines on periendoscopy management recommend the continuation of aspirin based on evidence from cohort studies, mostly retrospective, suggesting that the rate of bleeding is low. Cardiovascular complications from aspirin interruption can lead to disabilities and occasional deaths. The cardiovascular risks following aspirin continuation or interruption in endoscopy have not been well studied. There has been no randomized study to compare either strategy. Endoscopists are divided on their opinion on whether to stop or to continue aspirin. The proposed large randomized controlled trial (RCT) is powered to detect small differences in both outcomes. Findings from this RCT will address this important question and inform our clinical practice.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• patients receiving aspirin (80mg daily or more) for secondary prevention against cardiovascular diseases who require elective colonoscopy for colorectal cancer screening.

Locations
Other Locations
Hong Kong Special Administrative Region
Prince of Wales Hospital
RECRUITING
Hong Kong
Contact Information
Primary
James Yun Wong Lau, MD
laujyw@surgery.cuhk.edu.hk
+85235051445
Backup
Cecilia Chan, PhD
ceciliachan@surgery.cuhk.edu.hk
35052640
Time Frame
Start Date: 2026-02-10
Estimated Completion Date: 2031-12-31
Participants
Target number of participants: 2514
Treatments
Active_comparator: aspirin
8-day (-5, +3) supply of aspirin 80mg before and after colonoscopy
Placebo_comparator: Placebo
8-day (-5, +3) supply of placebo 80mg before and after colonoscopy
Sponsors
Leads: Chinese University of Hong Kong

This content was sourced from clinicaltrials.gov