Comparing robotic and hybrid methods for ventral hernia repair
Robotic Assisted vs. Laparoscopic Hybrid IPOM Ventral Hernia Repair: a Prospective Randomized Study Comparing Postoperative Outcomes
This study is testing whether a robotic method for fixing ventral hernias works better than a hybrid method in helping patients feel less pain and have fewer complications after surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | Kuopio University Hospital Academic / other |
| Locations | 1 site (Kuopio, Northern Savo) |
| Trial ID | NCT05233020 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of robotic-assisted ventral hernia repair (rVHR) compared to hybrid-assisted repair in patients with incisional ventral hernias sized between 3 to 6 cm. A total of thirty patients will be recruited, with fifteen undergoing each type of repair. The primary outcomes measured will include postoperative pain, hernia recurrence, and quality of life, assessed at multiple time points using visual analogue scales and the SF-36 questionnaire. The goal is to determine if rVHR can reduce complications associated with traditional laparoscopic methods.
Who should consider this trial
Good fit: Ideal candidates for this study are patients with incisional ventral hernias measuring between 3 to 6 cm.
Not a fit: Patients with a history of previous ventral hernia repairs will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved postoperative outcomes and quality of life for patients undergoing ventral hernia repair.
How similar studies have performed: Previous studies have shown promising results with robotic-assisted surgical techniques, suggesting potential benefits over traditional methods.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ventral hernia size 3-6 cm Exclusion Criteria: * previous ventral hernia
Where this trial is running
Kuopio, Northern Savo
- Kuopio University Hospital — Kuopio, Northern Savo, Finland (Recruiting)
Study contacts
- Principal investigator: Pirjo Käkelä, PhD — gi-surgeon, clinical teacher
- Study coordinator: Pirjo Käkelä, PhD
- Email: pirjo.kakela@kuh.fi
- Phone: 044 717 4796
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.