Antireflux Suture In One Anastomsis Gastric Bypass

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

Status

Recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07148492

Enrollment

316

Registered

2025-08-29

Start date

2024-01-01

Completion date

2025-09-30

Last updated

2025-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Reflux Disease, Gastro-Esophageal, Vomiting, Postoperative

Brief summary

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

PROCEDUREAntireflux suture

Antireflux suture will be taken in this intervention group

PROCEDURENo Antireflux suture

Antireflux suture will not be taken in this intervention group

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

Inclusion criteria

* Patients undergoing one anastomosis gastric bypass surgery

Exclusion criteria

* Non consenting individuals

Design outcomes

Primary

Measure	Time frame	Description
Reflux disease	3 months and 6 months postoperatively	The incidence of gastroesophageal reflux will be measured after surgery

Secondary

Measure	Time frame	Description
Postoperative vomiting	At 3 months and 6 months postoperatively	Incidence of postoperative vomiting will be measured

Countries

Pakistan

Contacts

Primary ContactSaeed Sarwar, MBBS

saeedkmc2020@gmail.com+923420973863

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026