Actively Recruiting
Cleansing Options in Out-Patient Setting to Improve Tolerance (COOP SIT) Trial
Led by Morehouse School of Medicine · Updated on 2025-10-09
300
Participants Needed
1
Research Sites
86 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this research is to compare patient preferences for two bowel preparation options: low-volume tablets (Suflave/Sutab) versus the standard colon preparation using Golytely (polyethylene glycol). The study aims to enroll approximately 300 patients, who will be randomly assigned to one of the two preparation methods in a 2:1 ratio prior to their scheduled colonoscopy appointments. Surveys will be conducted both before and after the procedures. This project will be conducted over a 12-month period and seeks to compare patient experience of both preparation methods in an outpatient setting. The study will evaluate the rate of preparation completion, patient satisfaction, tolerance of the solutions, and the endoscopic adequacy of each method. Eligible participants are patients aged 18 or older with upcoming colonoscopy appointments who can provide informed consent in English or Spanish. There is no health risks associated with this study, as both bowel preparation methods are FDA-approved and commonly used in clinical practice.
CONDITIONS
Official Title
Cleansing Options in Out-Patient Setting to Improve Tolerance (COOP SIT) Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults over age of 18 years undergoing outpatient colonoscopy for various indications
- Ability to consent in English or Spanish
- Patients with a history of colorectal cancer or previous surgery are allowed
You will not qualify if you...
- Patient is less than 18 years of age
- Pregnant or nursing women
- Unable to consent
- Patient is incarcerated
AI-Screening
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Trial Site Locations
Total: 1 location
1
Morehouse School of Medicine
Atlanta, Georgia, United States, 30310
Actively Recruiting
Research Team
J
Julia J Liu, MD, MSc
CONTACT
T
Tasha Rhymes, M.S. Ed.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
3
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