Clinical Trial

SetUp Study for HugoTM RAS Inguinal Hernia Repair

Study acronym: SUSHI
Completed
View on ClinicalTrials.gov →
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.
Protocol Amendment History 6 changes
critical Trial completed 2026-08-08
critical Phase changed: not applicable -> not specified 2026-08-08
notable Enrollment reduced: 100 -> 50 participants 2026-08-08
minor Trial arms changed: 2 -> 1 2026-08-08
notable Primary completion moved earlier: 2025-11-30 -> 2025-02-07 2026-08-08
minor Completion moved earlier: 2025-12-31 -> 2025-02-07 2026-08-08
Trial Details
NCT Number NCT06599515
Lead Sponsor Algemeen Ziekenhuis Maria Middelares
Conditions Inguinal Hernia
Enrollment 50 participants
Start Date 2023-09-15
Primary Completion 2025-02-07 (estimated)
Study Completion 2025-02-07 (estimated)
Updated on ClinicalTrials.gov 2026-08-07