University Hospitals Leuven
Leuven, Vlaams-Brabant, 3000, Belgium
NCT Number: NCT00925067
A randomized, prospective clinical trial analyzing whether the use of lightweight prostheses during laparoscopic inguinal hernia repair of male patients could have a beneficial effect on postoperative discomfort, chronic pain development, recurrence and male fertility aspects.
Looking for future studies?
Notify Me18 year–50 year
Male
Interventional
Not applicable
Leuven, Vlaams-Brabant, 3000, Belgium
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
laparoscopic inguinal hernia repair with a standard heavyweight Marlex (control group) prosthesis or new generation lightweight VyproII and TiMesh prostheses (study group)
Time frame: 12 months
Time frame: 1, 3, 6 and 12 months
Looking for future studies?
Notify MeUniversitaire Ziekenhuizen KU Leuven
Other
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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.
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