Stitch or clip? small trial aims to cut bleeding risk after Weight-Loss surgery
NCT ID NCT07238309
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests two common techniques—oversewing with stitches versus using surgical clips—to reinforce the staple line in gastric bypass surgery and reduce post-operative bleeding. Thirty adults undergoing laparoscopic one-anastomosis gastric bypass will be randomly assigned to one method. The main goal is to see which approach leads to fewer bleeding events within 30 days 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
- Oversewing and surgical ligation clips
- What this could lead to
- If this trial succeeds, it could show which technique better prevents bleeding after gastric bypass, improving patient safety and recovery.
- What could go wrong
- This is a small, early-stage trial with only 30 participants, so results may not apply to everyone. The methods are already in use, so no major new risks are expected.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2025
- Expected to finish
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Jun 2026
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.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * ✔ Age ≥ 18years old * Sex: both sex * Fit for bariatric surgery * body mass index (BMI) of 40 kg/m 2 or higher or BMI between 35 and 40 kg/m2 with significant comorbidities, such as T2DM, hypertension, OSAS or significant osteo- articular alterations, not responsive to medical therapies * Patients should have tried and failed to lose weight using diet, exercise, and/or medication for at least 6 months * Patients or first guardians accept to participate in the current study * Patients or first guardians accept to provide informed written consent Exclusion Criteria: * Patients less than 18 years old * Patients or first guardians refused to participate in the current study * Patients or first guardians refused to provide informed written consent * All patients with bleeding disorders and patients needing re-exploration for bleeding other than staple line Pregnant or breastfeeding women
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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
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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Faculty of Medicine, Cairo University
RECRUITINGCairo, Cairo Governorate, Egypt
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