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Comparison of anterior and posterior gastrojejunostomy in patients undergoing one anastomosis gastric bypass

Comparison of anterior and posterior gastrojejunostomy in patients undergoing one anastomosis gastric bypass: Randomized trial study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190128042520N11
Enrollment
82
Registered
2025-07-29
Start date
2025-07-23
Completion date
Unknown
Last updated
2025-08-19

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

Conditions

Condition 1: Dumping syndrome. Condition 2: Gastro-oesophageal reflux disease. Postgastric surgery syndromes Gastro-esophageal reflux disease

Interventions

Intervention 1: First intervention group: Posterior gastrojejunostomy (end-to-side) with Endo GIA linear stapler 40 mm at the transverse end of the gastric pouch. Intervention 2: Second intervention g

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with obesity (body mass index 40 to 50 kg/m2) in the age range of 18 to 65 years

Exclusion criteria

Exclusion criteria: History of bariatric or major abdominal surgery Significant underlying medical conditions (cardiac, pulmonary, hepatic, renal, or coagulation disorders) Severe psychiatric illness or inability to comply with follow-up Current pregnancy or planned pregnancy during the study period Severe gastroesophageal reflux disease (GERD grade C or D) Active substance or alcohol abuse

Design outcomes

Primary

MeasureTime frame
Sigstad questionnaire score for assessin, the Incidence and severity of dumping syndrome in patients undergoing single-anastomosis gastric bypass. Timepoint: 6 weeks, 3 months, 6 months, 12 months after surgery. Method of measurement: Sigstad's score questionnaire.;Score obtained from the standard GERD-Q questionnaire to measure the incidence and severity of symptoms of gastroesophageal reflux disease. Timepoint: 6 weeks, 3 months, 6 months, 12 months after surgery. Method of measurement: Standard GERD-Q questionnaire.;Upper gastrointestinal endoscopy findings to assess the incidence and severity of gastroesophageal reflux-related esophagitis. Timepoint: 12 months after surgery. Method of measurement: Upper gastrointestinal endoscopy.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Kermansaravi

Iran University of Medical Sciences

kermansaravi.m@iums.ac.ir+98 21 8871 7272

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026