Status:
COMPLETED
TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh
Lead Sponsor:
Medtronic - MITG
Conditions:
Postoperative Complications
Eligibility:
All Genders
18+ years
Brief Summary
The objective of this retrospective study is to evaluate the postoperative clinical outcomes at discharge, 1 month and 12 months, associated with the use of Parietex™ ProGrip™ in Laparoscopic Transabd...
Eligibility Criteria
Inclusion
- The following diagnosis will be included:
- Inguinal hernia: unilateral or bilateral
- All subjects must meet the following inclusion criteria:
- ≥18 years of age
- Had undergone elective (non-emergent) primary surgical repair of the above diagnosis with Parietex ProGrip™ by Laparoscopic Transabdominal preperitoneal inguinal hernia repair between September 2008 to March 2010
- Post-operative follow-up ≥ 12 months or recurrence which occurs within the 12 months post-surgery (If subject has a known incidence of recurrence before the 12 months follow up, the subject will be included in the study.)
Exclusion
- Subjects who meet any of the following exclusion criteria are not eligible for study participation:
- Patients with previous laparoscopic Inguinal hernia repair
- Emergency procedures
- Patients with incarcerated hernias
Key Trial Info
Start Date :
October 1 2011
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 1 2013
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT01481376
Start Date
October 1 2011
End Date
April 1 2013
Last Update
January 7 2016
Active Locations (1)
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1
Evangelisches Krankenhaus Zweibrücken - Obere Himmelsbergstr. 38
Zweibrücken, Germany, 66482