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Study identifier: NCT05488288 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Bariatric SUrgery With Mesh REpair of Ventral Hernia: a Randomized Controlled Trial

Condition: Ventral Hernia  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhasePhase 3
Planned participants354
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

The primary objective of the study is to demonstrate that hernia recurrence (VH) repair with non absorbable mesh concomitant to Bariatric Surgery (BS) decreases the risk of VH, with or without surgical repair, during the first two years after BS when compared to VH suture repair without mesh. As secondary objectives, the study aims to assess the impact of concomitant VH repair with non absorbable mesh versus suture repair in morbidly obese BS candidates on the following measures: - hernia recurrence at 1 year after randomization; - reoperation for hernia recurrence at 2 years after randomization; - strangulated hernia, surgical infection and mesh bulging at one year after randomization; - postoperative morbidity and mortality at 90 days after randomization; - benefit-risk ratio; - chronic pain at three months, six months, one year and two years after randomization; - quality of life during the two years after randomization; - incremental cost utility ratio; - short- and mid-term weight loss. To study if the efficacy of mesh versus suture VH repair differs according to the type and size of VH and to the surgical technique.

This description comes directly from the study's public registry record.

Talk to the study team

David MOSZKOWICZ, MD, PhD  ·  +33 (0)1 47 60 66 02  ·  david.moszkowicz@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Department of visceral and digestive surgery, Louis Mourier hospital, APHPColombes, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05488288