Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Bacteriologically controlled reusable water bottles for colonoscopy.

Official title: Evaluation of the Microbiological and Organizational Impact of the Use of Bacteriologically Controlled Water in COLOscopy for an Evolution of Our Practices Towards a More Ecoresponsible Endoscopic Activity COLO SOUS L'EAU

Run by University Hospital, Bordeaux · NCT06688955 · Data updated 2026-11-12

We will test whether using bacteriologically controlled reusable water bottles during colonoscopy is microbiologically safe for adults having scheduled colonoscopies at Bordeaux University Hospital.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment40 (estimated)
SponsorUniversity Hospital, Bordeaux
Academic / other
Locations1 site (Pessac)
StatusRecruiting
StartedSeptember 29, 2025
Main results expectedDecember 2025
Study endsDecember 2025
Registry record updatedOctober 3, 2025
Trial IDNCT06688955 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults scheduled for a colonoscopy in room 4 during the Monday or Tuesday morning shifts at CHU de Bordeaux who can give informed consent and are covered by social security.

Probably not a fit

Patients who are pregnant, require emergency colonoscopy, need indigo-carmine chromoendoscopy, are under guardianship, or lack social security coverage are excluded and would not benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Colonoscopy using the water-exchange technique requires about 1 L of water per patient and can improve scope progression, comfort, and polyp detection. This single-center interventional project at CHU de Bordeaux will use bacteriologically controlled water in reusable wash bottles and collect a 200 ml sample from each bottle after the procedure for bacteriological analysis. The study will also set up and assess a sterilization and reconditioning circuit for the bottles, gather staff feedback on feasibility and acceptability, and compare the carbon footprint and waste generation versus single-use sterile bottles. Findings will indicate whether the reusable-bottle process is microbiologically safe and operationally practical for wider adoption.

Why it matters

Potential benefit: If successful, this could let centers replace single-use sterile bottles with safe reusable bottles, reducing plastic waste and sterilization costs without increasing infection risk.

How similar studies have gone: While water-exchange colonoscopy is supported by international recommendations, the specific use of bacteriologically controlled water in reusable bottles has not been previously validated and remains largely untested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* All patients with a colonoscopy indication whose examination is scheduled in room 4, on a Monday and Tuesday shift (8:30 a.m. - 1:30 p.m.)
* Male or female of legal age at the time the colonoscopy is ordered
* Patient willing to participate in the study
* Person affiliated with or benefiting from a social security plan

Exclusion Criteria:

* Pregnant woman
* Patient of legal age under guardianship or protected person
* Patient requiring indigo-carmine chromoendoscopy
* Patient requiring an emergency colonoscopy
* Patient not affiliated to the social security system

Where it's running

  • CHU de Bordeaux - Hôpital haut Lévêque
    Pessac, France
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.