Robotic Single Port Combined Umbilical and Inguinal Hernia Repair
CAPPUCCINOH
Combined APProach of Umbilical ConComitant With Inguinal Hernia
1 other identifier
interventional
30
1 country
1
Brief Summary
Evaluation of the perioperative and patient reported outcomes of a new surgical technique: robotic inguinal hernia repair using the Da Vinci SP system.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Apr 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2026
CompletedFirst Submitted
Initial submission to the registry
August 5, 2026
CompletedFirst Posted
Study publicly available on registry
August 10, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2029
August 10, 2026
August 1, 2026
2 years
August 5, 2026
August 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Technical errors with the robotic system
Number and type of technical errors or device-related issues encountered during the procedure.
During surgery
Operative time
Total operative time from skin incision to skin closure
During surgery
Complication Rate
Intraoperative, in-hospital and postoperative complications classified according to the Clavien-Dindo classification
From surgery until 1 month postoperatively
Success rate
success rate of preperitoneal mesh placement
From surgery until planned follow-up 1 month potoperatively
Secondary Outcomes (3)
EuraHS Quality of Life score
Preoperatively, 1 month and 1 year postoperatively
Body Image Questionnaire Score
Preoperatively, 1 month , and 1 year postoperatively
Hernia recurrence
1 year postoperatively
Study Arms (1)
Robotic Single-Port Inguinal and Concomitant Umbilical Hernia Repair
EXPERIMENTALInterventions
Robotic surgical platform used to perform single-port robotic inguinal hernia repair with concomitant umbilical hernia repair through a single umbilical access site.
Robotic single-port inguinal hernia repair with concomitant umbilical hernia repair through a single umbilical access site using the da Vinci SP system.
Eligibility Criteria
You may qualify if:
- Adults with a primary inguinal hernia, either unilateral or bilateral, in association with a primary umbilical hernia of \>1
You may not qualify if:
- recurrent inguinal hernia after preperitoneal repair
- irreducible scrotal hernia
- post-prostatectomy
- laparotomy in the lower abdomen
- pregnancy
- contra-indication for general anaesthesia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
AZ Maria Middelares
Ghent, East-Flanders, 9000, Belgium
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head of Surgery Department
Study Record Dates
First Submitted
August 5, 2026
First Posted
August 10, 2026
Study Start
April 1, 2026
Primary Completion (Estimated)
April 1, 2028
Study Completion (Estimated)
April 1, 2029
Last Updated
August 10, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share