Single-Port Robotic Suprapubic Hernia Repair for Inguinal Hernias
Official title: Minimal ACCess Hernia InguinAlis Treatment of Hernia (MACCHIATOH Study): Prospective Cohort Study of Single-port Robotic Suprapubic Inguinal Hernia Repair (SPIN Procedure)
Run by Algemeen Ziekenhuis Maria Middelares · NCT07756749 · Data updated 2026-11-12
A new single-port robotic surgery (SPIN procedure) is being tested to repair primary inguinal hernias in adults to see if it works well and feels better for patients.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Algemeen Ziekenhuis Maria Middelares Academic / other |
| Locations | 1 site (Ghent, East-Flanders) |
| Status | Recruiting |
| Started | August 2, 2026 |
| Main results expected | August 2, 2028 |
| Study ends | August 1, 2029 |
| Registry record updated | September 4, 2026 |
| Trial ID | NCT07756749 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with a primary unilateral or bilateral inguinal hernia suitable for laparoscopic repair, without contraindications to general anesthesia.
✕Probably not a fit
Patients with recurrent hernias after prior repair, irreducible hernias, or conditions preventing general anesthesia may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study is a prospective, single-centre, single-arm cohort evaluating a novel SPIN technique for primary inguinal hernias. Participants undergo a suprapubic, single-port robotic repair using the da Vinci SP system, with 12 months of follow-up to monitor safety, effectiveness, and patient-reported outcomes. The goal is to determine whether SPIN provides safe surgery with acceptable recovery, similar or better pain control, cosmesis, and satisfaction compared with existing minimally invasive methods. The study enrolls 30 consecutive patients and excludes those with prior complex hernias or contraindications to general anesthesia. Results from this IDEAL Stage 2b study will inform feasibility, potential benefits, and future comparative research.
Why it matters
Potential benefit: If successful, SPIN could offer safe repair with reduced pain, better cosmetic results, and high patient satisfaction for primary inguinal hernias.
How similar studies have gone: Previous single-port approaches exist, but this specific suprapubic SPIN technique is novel and its efficacy is being explored in this IDEAL Stage 2b study.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
-
AZ Maria Middelares
Ghent, East-Flanders, Belgium Recruiting
Study contacts
- Study coordinator: Filip Muysoms, MD, PhD
- Email: filip.muysoms@gmail.com
- Phone: +32477325710
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.