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Completed NCT06599515

SetUp Study for HugoTM RAS Inguinal Hernia Repair

Conditions: Inguinal Hernia

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: Yes
Enrollment: 50
Sponsor: Algemeen Ziekenhuis Maria Middelares

Location: AZ Sint-Vincentius Deinze

Summary

The goal of this observational cohort study is to evaluate the evolution of the operative time in performing robotic-assisted laparoscopic inguinal hernia repair (rTAPP) during the learning curve of the first 50 patients using the HugoTM Ras (Medtronic) robotic system using the setup guide. This will be compared to the operative time for rTAPP in 50 patients performed by the same surgeon in another hospital. This data was collected in an earlier similar study with the start of the experience using the daVinci Xi (Intuitive Surgical) robotic system.

Eligibility Criteria

Inclusion Criteria: All patients planned for a minimal invasive (robotic assisted laparoscopic) inguinal hernia repair during the study period will be invited to take part in the study. Both unilateral and bilateral hernias will be included. Exclusion Criteria: * Recurrent hernias after previous preperitoneal mesh placement. * Inguinal hernias after abdominal prostatectomy. * Pregnancy. * Emergency surgery. * Age below 18 years. * Absence of informed consent.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06599515). StuddyBuddy aggregates publicly available trial information.