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Recruiting NCT07148492

Antireflux Suture In One Anastomsis Gastric Bypass

No phase Interventional Reflux Disease, Gastro-Esophageal Vomiting, Postoperative

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Antireflux suture, No Antireflux suture.
Who it may be relevant to
Registry conditions: Reflux Disease, Gastro-Esophageal, Vomiting, Postoperative. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Antireflux Suture In Laparoscopic One Anastomsis Gastric Bypass Surgery, A Randomised Control Trial

Overview

To prevent refulx symptoms in a type of bariatric surgery, a suture is taken.there is no enough evidence in support of or against the suture. our study aims to compare the symptoms of patients in whom the suture is taken and in those in whom it is not.

Interventions

  • Procedure Antireflux suture
    Antireflux suture will be taken in this intervention group
  • Procedure No Antireflux suture
    Antireflux suture will not be taken in this intervention group

Primary outcome measures

  • Reflux disease [Time frame: 3 months and 6 months postoperatively]
Secondary outcome measures (1)
  • Postoperative vomiting [Time frame: At 3 months and 6 months postoperatively]

Eligibility criteria

Inclusion criteria

  • Patients undergoing one anastomosis gastric bypass surgery

Exclusion criteria

  • Non consenting individuals

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Prevention

Study locations

Pakistan · 1 center
  • Khyber teaching hospital — Peshawar

Identifiers

NCT: NCT07148492 · 528/DME/KMC

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗