Elective sigmoid resection for recurrent diverticulitis: does it help bowel function and quality of life?

Is this trial a fit for you?

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

What this trial studies

This observational assessment compares outcomes after elective sigmoidectomy versus conservative management in patients with recurrent uncomplicated sigmoid diverticulitis. It aims to clarify how surgery affects bowel function and overall quality of life, informing guidelines for individualized treatment decisions. The study acknowledges international variation in recommendations and focuses on patient-centered outcomes beyond the number of acute episodes. Data collection includes clinical history, surgical indications, and QoL measures to identify which patients benefit most from surgery. Participation is limited to adults undergoing planned elective resection or conservative care at the Basel site.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients with recurrent uncomplicated diverticulitis and surgical indication for sigmoid resection
* Patients with recurrent uncomplicated diverticulitis and non-surgical indication for conservative management
* Confirmation of at least one episode of acute uncomplicated diverticulitis in computed tomography

Exclusion Criteria:

* Patients aged under 18.
* Patients unable to understand an informed consent.
* Patients with chronic pain disorder.
* Patients with sigmoid fistulas
* Emergency operations.
* Pregnant women or lactation.
* Patients with other severe gastrointestinal diseases, such as inflammatory bowel diseases (IBD), carcinoma or immunologic disorders.
* Patients unable to perform surgery or high-risk patients according to the American Society of Anesthesiology (ASA 4 grade or higher)

Where it's running

• St. Claraspital Basel
  Basel, Switzerland Recruiting

Study contacts

• Principal investigator: Daniel Steinemann, MD — Clarunis
• Study coordinator: Bettina Wölnerhanssen, MD
• Email: bettina.woelnerhanssen@claraspital.ch
• Phone: 0041616858585

Similar studies

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

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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.