Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT07238309

Efficacy of Oversewing Versus Surgical Ligation Clips for Staple Line Reinforcement of the Gastric Pouch to Reduce Post Operative Bleeding in Laparoscopic One Anastomosis Gastric Bypass

Led by Cairo University · Updated on 2025-11-20

30

Participants Needed

1

Research Sites

54 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

1. To test if there is a significant differences between Oversewing versus surgical ligation clips for staple line reinforcement of the gastric pouch regarding the reduction of post operative bleeding and the need for blood transfusions in laparoscopic one anastomosis gastric bypass. 2. To assess whether oversewing or the use of surgical clips is more effective in reducing operative time and Cost analysis in (OAGB). 3. To Provide evidence-based recommendations on staple line reinforcement techniques in OAGB, emphasizing patient safety and procedural efficiency

CONDITIONS

Official Title

Efficacy of Oversewing Versus Surgical Ligation Clips for Staple Line Reinforcement of the Gastric Pouch to Reduce Post Operative Bleeding in Laparoscopic One Anastomosis Gastric Bypass

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Both sexes eligible
  • Fit for bariatric surgery
  • Body mass index (BMI) of 40 kg/m2 or higher, or BMI between 35 and 40 kg/m2 with significant comorbidities such as type 2 diabetes, hypertension, obstructive sleep apnea syndrome, or serious osteo-articular problems not responding to medical treatment
  • Failed weight loss attempts using diet, exercise, and/or medication for at least 6 months
  • Patients or guardians agree to participate in the study
  • Patients or guardians provide written informed consent
Not Eligible

You will not qualify if you...

  • Age under 18 years
  • Patients or guardians refuse to participate
  • Patients or guardians refuse to provide written informed consent
  • Bleeding disorders
  • Need for re-exploration due to bleeding unrelated to the staple line
  • Pregnant or breastfeeding women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Faculty of Medicine, Cairo University

Cairo, Cairo Governorate, Egypt

Actively Recruiting

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Research Team

S

Sameh Gamal Abd Elghany, MSc

CONTACT

G

George AbdElFady Nashed Aiad, M.D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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