The aim of the present study is to analyse the feasibility, safety and IH rate using a prophylactic sublay biosynthetic BIO-A (GORE) mesh in order to prevent incisional hernia following midline laparotomy in clean-contaminated and contaminated wounds. The study was designed as a double-blind randomized controlled trial comparing the running suture alone to the running suture reinforced with biosynthetic mesh (BIOA) in sub lay position.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Rate of Incisional Hernia at Ultrasound examination
Timeframe: 3 months
Rate of Incisional Hernia at Ultrasound examination
Timeframe: 6 months
Rate of Incisional Hernia at Ultrasound examination
Timeframe: 12 months
Rate of Incisional Hernia at Ultrasound examination
Timeframe: 24 months
Rate of Incisional Hernia at Clinical examination
Timeframe: 3 months
Rate of Incisional Hernia at Clinical examination
Timeframe: 6 months
Rate of Incisional Hernia at Clinical examination
Timeframe: 12 months
Rate of Incisional Hernia at Clinical examination
Timeframe: 24 months