Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 18 and up

Oral Bisacodyl Before Catheter Insertion to Help Peritoneal Dialysis

Official title: Multi-Centre Pragmatic Randomized Controlled Trial of Bowel Preparation Before Peritoneal Dialysis Catheter Insertion

Run by Chinese University of Hong Kong · NCT07351357 · Data updated 2026-11-12

This study tests whether giving a laxative before Tenckhoff catheter insertion helps keep the catheter flowing smoothly for people starting peritoneal dialysis.

Quick facts

PhasePhase 4
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment398 (estimated)
SponsorChinese University of Hong Kong
Academic / other
Locations6 sites (Kwai Chung, Kowloon and 5 other locations)
StatusRecruiting
StartedJanuary 12, 2026
Main results expectedAugust 30, 2027
Study endsSeptember 30, 2027
Registry record updatedOctober 21, 2026
Trial IDNCT07351357 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older with kidney failure requiring peritoneal dialysis and scheduled for Tenckhoff catheter insertion.

Probably not a fit

Patients who do not experience dysfunction or who cannot tolerate laxatives may not benefit.

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

What this trial studies

This is a multicenter, open-label randomized controlled trial comparing laxative bowel preparation with standard care before Tenckhoff catheter placement for peritoneal dialysis. The goal is to see if prophylactic bisacodyl reduces catheter dysfunction that requires intervention after surgery. The trial plans to enroll about 199 patients per arm to detect a difference in catheter flow problems between 10% and 20% with 80% power. Primary outcome is catheter dysfunction requiring simple intervention. The study is conducted under the Chinese University of Hong Kong with three Hong Kong hospitals as sites.

Why it matters

Potential benefit: If successful, patients may experience fewer catheter flow problems and fewer interventions after catheter placement.

How similar studies have gone: Other similar approaches have shown potential to reduce postoperative catheter issues, but this specific prophylactic laxative strategy is novel in this setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* aged 18 or older and need of peritoneal dialysis
* willingness to give written consent and comply with the study protocol

Exclusion Criteria:

* known contraindication to peritoneal dialysis
* ongoing diarrhoea or active inflammatory bowel disease
* participation in another interventional study within last 30 days of randomization
* history of a psychological illness or condition that would interfere with the patient's ability to understand the requirement of the study and/or comply with the dialysis procedures

Where it's running

  • Prince of Wales Hospital
    Shatin, Nt, Hong Kong
    Recruiting
  • Princess Margaret Hospital
    Kwai Chung, Kowloon, Hong Kong
    Not yet recruiting
  • Caritas Medical Centre
    Sham Shui Po, Kowloon, Hong Kong
    Not yet recruiting
  • Tseung Kwan O Hospital
    Tseung Kwan O, Nt, Hong Kong
    Not yet recruiting
  • Queen Elizabeth Hospital
    Yau Ma Tei, Nt, Hong Kong
    Not yet recruiting
  • Prince of Wales Hospital
    Shatin, Hong Kong
    Not yet recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.