NCT03445936View on ClinicalTrials.gov

PRELOOP Trial: Synthetic Versus Biological Mesh for Prevention of Incisional Hernia After Loop-ileostomy Closure

NAActive, not recruitingINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

February 13, 2018

Primary Completion Date

October 30, 2022

Study Completion Date

October 31, 2027

Conditions
Rectum Cancer
Interventions
DEVICE

Parietene Macro

Parietene Macro is placed and sutured on retro muscular space on closed posterior rectus sheath to prevent incisional hernia.

DEVICE

Permacol

Permacol biologic implant is placed and sutured on retro muscular space on closed posterior rectus sheath to prevent incisional hernia.

Trial Locations (4)

Unknown

Jyvaskyla Central Hospital, Jyväskylä

Oulu University Hospital, Oulu

Seinajoki Central Hospital, Seinäjoki

Tampere University Hospital, Tampere

All Listed Sponsors
lead

University of Oulu

OTHER

NCT03445936 - PRELOOP Trial: Synthetic Versus Biological Mesh for Prevention of Incisional Hernia After Loop-ileostomy Closure | Biotech Hunter | Biotech Hunter