Evaluation of the perioperative and patient reported outcomes of a new surgical technique: single-port robotic suprapubic inguinal hernia repair (SPIN procedure).
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Adults with a primary inguinal hernia, either unilateral or bilateral
Exclusion Criteria:
* Recurrent inguinal hernia after preperitoneal repair
* Irreducible scrotal hernia
* Post-prostatectomy
* Laparotomy in the lower abdomen
* Pregnancy
* Contra-indication for general anaesthesia
Primary outcome measure(s)
Operative time — During surgery Total operative time from skin incision to skin closure
Technical errors with the robotic system — During surgery Number and type of technical errors or device-related issues encountered during the procedure.
Complication Rate — From surgery until 1 month postoperatively Intraoperative, in-hospital and postoperative complications classified according to the Clavien-Dindo classification
Trial sites (1)
Facility
City
Region
Status
AZ Maria Middelares
Ghent
East-Flanders
Recruiting
More Algemeen Ziekenhuis Maria Middelares trials in Belgium
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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