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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00498810
Other study ID # 2007/241
Secondary ID
Status Terminated
Phase N/A
First received July 9, 2007
Last updated January 27, 2011
Start date September 2007
Est. completion date January 2008

Study information

Verified date January 2011
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Terminated
Enrollment 160
Est. completion date January 2008
Est. primary completion date January 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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- All patients with mesh placed intra-abdominally during surgery have to be withdrawn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

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
complete repair

partial repair of the abdominal wall


Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary recurrence rate 1 year
Secondary Perioperative morbidity rate
Secondary Postoperative pain
Secondary Long term complication rate
Secondary Recurrence rate 3 years
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