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Clinical Trial Summary

Patients undergoing laparoscopic sleeve gastrectomy will be randomized into 2 groups. In one group, a staple line inversion with a running suture of Polypropylene will be performed. In the second group, the gastric section will be performed with a stapler with preloaded buttress material

Postoperative nausea and vomits during the first 24 hours will be investigated.


Clinical Trial Description

Patients undergoing laparoscopic sleeve gastrectomy as bariatric procedure will be randomized into 2 groups. In one group after the stapling and section of the stomach with stapling devices (EndoGIA, Covidien, USA), a staple line inversion with hemostatic and aims will be performed. Staple line inversion will be performed with a running suture of Polypropylene 2/0. In the second group, the gastric section will be performed with a stapler with preloaded buttress material (EndoGIA with reinforced reload, Covidien, USA).

Postoperative nausea and vomits during the first 24 hours after surgery will be investigated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03104023
Study type Interventional
Source Hospital General Universitario Elche
Contact Lorea Zubiaga, MD, PhD
Email obesidadhospitalgeneralelche@gmail.com
Status Recruiting
Phase Phase 3
Start date January 2017
Completion date August 2017

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