Clin2
NCT07761884Possibly a fitNot yet recruiting

Sacral nerve stimulation for bowel control after rectal cancer surgery

Low Anterior Resection Syndrome (LARS)

Part of Digestive system clinical trials.

This trial tests whether a device that sends gentle electrical pulses to the sacral nerve can improve bowel control in people who have urgency or leakage after rectal cancer surgery.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
40 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years or older and can give informed consent.
  • You had rectal cancer surgery with the remaining bowel reconnected (anastomosis), with or without a temporary ileostomy that has been closed.
  • You have more than 6 episodes of urgency or bowel leakage in two weeks, as recorded in a daily diary.
  • Your LARS score is above 21, meaning you have moderate to severe bowel dysfunction after rectal surgery.
  • You do not have cancer spread (metastasis), are not undergoing chemotherapy, and do not have an ileostomy at the time of the study.
  • You do not have a pacemaker, active infection, allergy to implant materials, active inflammatory bowel disease, or had other bowel resections besides the rectal surgery.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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