Warm water trick cuts bleeding after gastric sleeve surgery
NCT ID NCT07475169
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested if using warm saline (body temperature) to rinse the stomach staple line during laparoscopic sleeve gastrectomy could reduce early bleeding after surgery. 200 adults having weight-loss surgery were randomly assigned to receive either warm or room-temperature saline. The goal was to see if this simple, low-cost change could lower the risk of bleeding, the need for blood transfusions, or additional procedures. The approach is easy to apply and may improve early recovery.
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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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200 people
The number who actually took part.
- Started
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Dec 2024
- Finished
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Jun 2025
- 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 60 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age between 18 and 60 years * BMI ≥ 40 kg/m², or BMI ≥ 35 kg/m² with at least one obesity-related comorbidity (e.g., type 2 diabetes, hypertension, obstructive sleep apnea) * Eligible for primary laparoscopic sleeve gastrectomy * Provided written informed consent Exclusion Criteria: * Previous major upper abdominal surgery with expected adhesions * Known bleeding disorders * Use of anticoagulant or antiplatelet therapy within 7 days before surgery * Advanced hepatic or renal disease * Unstable cardiac conditions * Pregnancy * Immunosuppression * Active systemic infection * Inability to comply with follow-up schedule
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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.
Contacts and locations
Locations
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Ain Shams University
Cairo, Egypt
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Other studies related to the condition(s) this trial covers.
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