NCT04311788View on ClinicalTrials.gov

Preemer Trial - Prophylactic Mesh Versus no Mesh in the Midline Emergency Laparotomy Closure for Prevention of Incisional Hernia: a Multi Center, Double-blind, Randomized Controlled Trial

NAActive, not recruitingINTERVENTIONAL
Enrollment

109

Participants

Timeline

Start Date

April 27, 2020

Primary Completion Date

February 3, 2025

Study Completion Date

March 31, 2028

Conditions
Incisional HerniaEmergency LaparotomyMidline LaparotomyHernia Prevention
Interventions
DEVICE

Prophylactic self gripping mesh

Prophylactic self gripping mesh, Propgrip by Medtronic.

DEVICE

Slowly absorbable continuous monofilament suture

Fascial closure by continuous slowly absorbable 4:1 suture

Trial Locations (7)

Unknown

Jorvi Hospital, Espoo

Helsinki University Hospital, Helsinki

Lahti Central Hospital, Lahti

Oulu University Hospital, Oulu

Seinäjoki Central Hospital, Seinäjoki

Tampere University Hospital, Tampere

Turku University Hospital, Turku

All Listed Sponsors
collaborator

Helsinki University Central Hospital

OTHER

lead

University of Oulu

OTHER