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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04115150
Other study ID # 1258/2018
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2011
Est. completion date September 1, 2018

Study information

Verified date October 2019
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hernia repair in sublay technique is widely accepted for ventral hernias, as it appears to be advantageous in terms of complication and recurrence rates. Recently, self-gripping meshes are increasingly used for hernia repair with retromuscular mesh positioning. However, real-life data on the safe use in that specific indication are still lacking. Therefore, this study evaluated short-term postoperative outcome of self-gripping versus conventional non-self-gripping meshes in sublay hernia repair.


Recruitment information / eligibility

Status Completed
Enrollment 244
Est. completion date September 1, 2018
Est. primary completion date July 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

- ventral hernia repair in sublay technique

Exclusion Criteria:

- ventral hernia repair in other technique

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Outcome

Type Measure Description Time frame Safety issue
Primary Complication rate overall complication rate, seroma rate, SSI rate 1 year