Can a new surgical stitch keep Crohn's disease at bay?

NCT ID NCT07772037

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time

Summary

This study looks at tissue samples from people with Crohn's disease who had bowel surgery, comparing two ways surgeons reconnect the intestine: the newer Kono-S technique and the standard method. The goal is to see if differences in a protective protein called GPX4, which helps shield cells from damage, explain why Crohn's disease often returns near the surgical join. By examining archived samples from 25 patients, researchers hope to uncover clues that could help surgeons pick the best technique and reduce the chance of disease coming back.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Surgical technique: Kono-S anastomosis versus conventional anastomosis
What this could lead to
If successful, this could help surgeons choose the best bowel-joining technique for each Crohn's patient and guide new treatments to improve healing and reduce disease recurrence.
What could go wrong
This is a small, retrospective pilot study, so findings may not apply broadly. It looks at tissue markers, not direct patient outcomes, and cannot prove cause and effect.

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

About 25 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Nov 2026

An estimate. Start dates often move.

Expected to finish

Nov 2027

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Crohn's disease undergoing ileocolic resection, for whom suitable archived histopathology material and relevant clinical data are available.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria:• Adults (≥18 years) with confirmed Crohn's disease who underwent ileocolic or small bowel resection with a primary anastomosis. * Documented anastomotic configuration (Kono-S or conventional). * Availability of archived pathology material from the resection specimen containing the anastomotic site. * At least one additional tissue timepoint available: preoperative endoscopic biopsy or follow up endoscopic biopsy within 24 months. * Available postoperative endoscopic follow up data (Rutgeerts score) where applicable. Exclusion Criteria: * • Indeterminate colitis or non-Crohn's pathology on histology. * Lack of retrievable tissue or poor tissue quality (e.g., extensive necrosis or autolysis) precluding IHC. * Unclear anastomotic type. * Absence of epithelial component in the available tissue (e.g., only serosa or fibrofatty tissue). * Major confounders that could affect GPX4 expression, such as severe ischaemia, uncontrolled sepsis, or immediate reoperation at the anastomotic site. * Patients with permanent stomas and no anastomotic follow up where interpretation would be ambiguous.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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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  3. A doctor treating you

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Contacts and locations

Locations

  • Queen Elizabeth the Queen Mother Hospital

    Margate, Kent, CT9 4AN, United Kingdom

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