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Life sciences · Interventional Study
ClinicalTrials.gov · October 2, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07854613). This is a study registration, not published results. Lead sponsor: China-Japan Friendship Hospital. Recruitment status: NOT_YET_RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 140 participants (ESTIMATED). Conditions: Omentopexy, Sleeve Gastrectomy, Gastroesophageal Reflux Disease. Interventions: PROCEDURE: Sleeve Gastrectomy With Omentopexy; PROCEDURE: Sleeve Gastrectomy. Primary outcome measures: Prevalence of de novo postoperative gastroesophageal reflux disease (GERD) , 12 months after surgery. Brief summary: The goal of this clinical trial is to compare the effects of sleeve gastrectomy with and without omentopexy on gastroesophageal reflux disease (GERD) in patients with obesity. The main question it aims to answer is: Does the addition of omentopexy to sleeve gastrectomy reduce the incidence of postoperative GERD compared with sleeve gastrectomy alone, as measured by the proportion of participants with a postoperative GERD-Q score ≥8? Researchers will compare sleeve gastrectomy with omentopexy to sleeve gastrectomy without omentopexy to determine whether omentopexy reduces the incidence of postoperative GERD. Participants will: Undergo sleeve gastrectomy with or without omentopexy according to their randomized treatment assignment. Complete the GERD-Q questionnaire after surgery to assess gastroesophageal reflux symptoms. Attend postoperative follow-up visits for assessment of GERD and other clinical outcomes.