Can we predict who recovers bowel and bladder control after rectal surgery?
NCT ID NCT05257746
First seen Aug 27, 2026 · Last updated Aug 28, 2026 · Updated 1 time
Summary
This study follows 500 people who have surgery to remove the rectum, a procedure called rectal resection. Researchers want to see how bowel and bladder function change before and after the operation, using questionnaires and pressure measurements. They will track patients for up to five years to identify risk factors for long-term problems with continence and sexual function. The goal is to help doctors spot who might need extra care or a different recovery plan after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Rectal resection with total mesorectal excision (a surgical procedure to remove the rectum)
- What this could lead to
- If this study succeeds, it could help doctors predict which patients are more likely to have lasting bowel or bladder problems after rectal surgery, and guide them toward extra support or different follow-up care.
- What could go wrong
- This is an observational study, so it cannot prove that any treatment works. The results depend on patients reporting their symptoms accurately, and the findings may not apply to everyone having rectal surgery.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 500 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2021
- Expected to finish
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Jun 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
All patients undergoing rectal resection with total mesorectal excision
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients undergoing rectal resection with total mesorectal excision Exclusion Criteria: * primary or secondary removal of rectal sphincter apparatus * patients with enterostomy persisting 12 months after initial rectal resection
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Department of Gastrointestinal-, Thoracic and Vascular Surgery University Hospital Carl Gustav Carus Technische Universität Dresden
RECRUITINGDresden, Saxony, 01307, Germany
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