Clinical Trial

Prevention of Petersen's Hernia After Laparoscopic Gastrectomy

Active, Not Recruiting
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Summary
* Aim of this study To compare the cases underwent operation to treat intestinal obstruction caused by Peterson hernia within 3 years after laparoscopic gastrectomy between closure method and Mefix methods. * Primary end point: The cases underwent operation to treat intestinal obstruction caused by Peterson hernia within 3 years after laparoscopic gastrectomy was not- inferior between Closure and MEFIX. * Secondary endpoint: Procedures' times (minutes), bleeding, Hospital stays (days) Occurrence of postoperative small bowel obstruction within 30 days after surgery, Short-term complications within 30 days after surgery, Occurrence of Petersen's Hernia according to the use of anti-adhesion agents, anastomotic methods, CLOSURE or MEFIX previous surgical suture condition, hernia degree, and bowel condition (strangulation, perforation) at the timing of emergent operation for treatment of Petersen's Hernia obstructions
Protocol Amendment History 5 amendments
This ClinicalTrials.gov record has been amended 5 times since 2021-10-22; most recent amendment 2025-03-11.
Status change: Recruiting → Active, Not Recruiting 2024-02-27
Status change: Not Yet Recruiting → Recruiting 2023-10-11
Trial Details
NCT Number NCT05105360
Lead Sponsor Gyeongsang National University Hospital
Collaborators: Medtronic
Conditions Petersen's Hernia
Enrollment 444 participants
Start Date 2022-04-01
Primary Completion 2027-01-26 (estimated)
Study Completion 2029-01-26 (estimated)
Updated on ClinicalTrials.gov 2025-03-13