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COMplete Versus PArtial Open inCisional Hernia Repair (COMPAC-TRIAL)

Not Applicable
Terminated
Conditions
Incisional Hernia
Registration Number
NCT00498810
Lead Sponsor
University Hospital, Ghent
Brief Summary

To compare the complete repair of the abdominal wall at the level of the former incision with only a partial repair at the level of the hernia in patients with an incisional hernia after median laparotomy in a prospective randomized trial.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
160
Inclusion Criteria
  • Written informed consent from the patient or his/her legal representative
  • Incisional hernia requiring elective surgical repair
Exclusion Criteria
  • No written informed consent
  • Emergency surgery (incarcerated hernia)
  • All incisional or parastomal hernias not originating at the midline
  • All recurrent hernias
  • All patients with mesh placed intra-abdominally during surgery have to be withdrawn

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
recurrence rate1 year
Secondary Outcome Measures
NameTimeMethod
Perioperative morbidity rate
Postoperative pain
Long term complication rate
Recurrence rate3 years

Trial Locations

Locations (1)

University Hospital Ghent

🇧🇪

Ghent, Belgium

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