The aim of the present study is to analyse feasibility, safety and Incisional Hernia rate using a prophylactic sub lay non-absorbable mesh \[Parietex Progrip (Medtronic) \] in order to prevent Incisional Hernia following midline emergent laparotomy in clean and clean-contaminated wounds.
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Rate of Incisional Hernia at Clinical examination
Timeframe: Patients are postoperatively examined at 3 months.
Rate of Incisional Hernia at Clinical examination
Timeframe: Patients are postoperatively examined at 6 months.
Rate of Incisional Hernia at Clinical examination
Timeframe: Patients are postoperatively examined at 12 months.
Rate of Incisional Hernia at Clinical examination
Timeframe: Patients are postoperatively examined at 24 months.
Rate of Incisional Hernia at Ultrasound examination
Timeframe: Patients are postoperatively examined at 3 months.
Rate of Incisional Hernia at Ultrasound examination
Timeframe: Patients are postoperatively examined at 6 months.
Rate of Incisional Hernia at Ultrasound examination
Timeframe: Patients are postoperatively examined at 12 months.
Rate of Incisional Hernia at Ultrasound examination
Timeframe: Patients are postoperatively examined at 24 months.