Trials / Not Yet Recruiting
Not Yet RecruitingNCT07361575
Study Comparing the Quality of Colon Cleanliness With Prepackaged LRD (Low-residue Diet) vs. Guided (POG).
A Single-blind, Randomized Study Comparing the Quality of Colon Cleanliness With Prepackaged LRD (Low-residue Diet) vs. Guided (POG).
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 230 (estimated)
- Sponsor
- Clinique Paris-Bercy · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Low-residue diet (LRD) in patient improves the quality of the colon cleanliness and thus the adenoma detection rate (ADR). This is a key criterion in colonoscopy screening for colorectal cancer (CRC). The benefit of an LRD lasting more than 24 hours before colonoscopy has not been demonstrated compared to a 24-hour LRD. Few studies have evaluated the benefit of a prepackaged 24-hour LRD compared to simply receiving oral and written LRD instructions during a consultation. The aim of the study is to evaluate the usefulness of a prepackaged LRD (Colobox®) compared to simple LRD instructions on colon cleanliness (Boston score) in patients examined by endoscopy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Colonoscopy | Colonoscopy performed and Boston score evaluated |
| OTHER | Questionnaires | LRD satisfaction questionnaire LRD compliance questionnaire |
| OTHER | Pre-colonoscopy diet according to the investigator's oral instructions | 24 hours before the colonoscopy, The patients follow a special diet, either by themselves according to the investigator's oral instructions |
| OTHER | Pre-colonoscopy diet by following a special preparation, Colobox. | 24 hours before the colonoscopy, The patients follow a special diet, by following a special preparation, Colobox. |
Timeline
- Start date
- 2026-01-30
- Primary completion
- 2026-11-15
- Completion
- 2026-11-30
- First posted
- 2026-01-23
- Last updated
- 2026-02-17
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT07361575. Inclusion in this directory is not an endorsement.