Medical University Innsbruck
Innsbruck, Tyrol, 6020, Austria
Completed
NCT Number: NCT02123719
Laparoscopic Incisional Hernia Repair in Liver Transplant Patients
Retrospective analysis of patients undergoing laparoscopic incisional hernia repair.
Study group: Patients with incisional hernia post liver transplantation Control group: Patients with incisional hernia post any other laparotomy in the upper quadrant.
Primary study outcome parameter: Risk of hernia recurrence. Secondary study outcome parameters: - Hernia repair-related infection rate
- Postoperative morbidity Statistical analysis: Comparison of study versus control group, univariate and multivariate analysis, Chi² and Mann-Whitney-U tests. P-values <0.05 were considered significant.
Completed
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Notify MeKey information
Age range
18 year–80 year
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Incisional hernia
- Laparoscopic repair possible
Exclusion criteria
- Other types of ventral hernias
- Laparoscopy not possible
Treatment and study plan
SURGERY
OtherPrimary outcomes
-
Hernia recurrence post laparoscopic incisional hernia repair
Time frame: 1 - 74 months post surgery
Sponsors and collaborators
Lead sponsor
Medical University Innsbruck
Other
Registry information
Official study title
Outcomes Analysis of Laparoscopic Incisional Hernia Repair and Risk Factors for Hernia Recurrence in Liver Transplant Patients
Important dates
- Study start
- 2013
- Primary completion
- 2013
- Study completion
- 2014
- First posted
- Apr 25, 2014
- Registry last updated
- Apr 25, 2014
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.