Assessment of Intra-abdominal Pressure During the Perioperative Period of Hernia Repair

Recruiting N/A Interventional Study
Hernia Incisional
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
10 (estimated)
Sponsor
Centre Hospitalier Universitaire de Nice · Other
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About This Trial
Thousands of patients worldwide undergo abdominal surgery every day; 2-11% of laparotomies will progress to an incisional hernia, particularly midline laparotomies, which are associated with higher hernia rates, reaching up to 70% in obese patients (1,2). Long-term recurrence after incisional hernia repair is close to 30% after primary repair and may increase to 70% in cases of iterative (redo) su…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Midline incisional hernias with a hernia defect width between 4 and 10 cm in the transverse axis, corresponding to W2 according to the EHS classification * M2, M3, and M4 locations according to the EHS classification (i.e., hernia defects located from 3 cm below the xiphoid pr…
Contacts

Damien MASSALOU, MD PhD

+33492032264

massalou.d@chu-nice.fr

CONTACT