Measuring abdominal wall tension during ventral hernia repair
Abdominal Wall Tension in Patients Undergoing Ventral Hernia Repair Without Component Separation
The Cleveland Clinic · NCT06051578
This study is testing a new way to measure the tightness of the abdominal wall during ventral hernia repair to see how it affects patients' recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | The Cleveland Clinic (other) |
| Locations | 1 site (Cleveland, Ohio) |
| Trial ID | NCT06051578 on ClinicalTrials.gov |
What this trial studies
This observational study aims to measure the tension of the abdominal wall in patients undergoing ventral hernia repair without component separation. Using an investigational tension scale attached to surgical clamps, surgeons will assess the abdominal wall tension during the procedure. The study will also explore patient factors that may contribute to variations in tension and examine the relationship between tension measurements and patient outcomes. Conducted at the Cleveland Clinic, this prospective cohort study involves experienced hernia surgeons.
Who should consider this trial
Good fit: Ideal candidates include patients scheduled for ventral hernia repair without component separation and those with midline hernias.
Not a fit: Patients with prior component separation, isolated flank hernias, or those under 18 years old may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical techniques and outcomes for patients undergoing ventral hernia repair.
How similar studies have performed: While this approach is innovative, similar studies focusing on abdominal wall tension in hernia repairs have not been widely reported, making this a novel investigation.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients who are planned to undergo ventral hernia repair without component separation 2. Midline hernia Exclusion Criteria: 1. Mesh excision for reasons other than mesh infection 2. Prior component separation 3. Isolated flank hernia 4. Patients under the age of 18 years 5. Pregnant patients
Where this trial is running
Cleveland, Ohio
- Cleveland Clinic Foundation — Cleveland, Ohio, United States (RECRUITING)
Study contacts
- Principal investigator: Benjamin Miller, MD — The Cleveland Clinic
- Study coordinator: Benjamin Miller, MD
- Email: millerb35@ccf.org
- Phone: 2164068573
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.
Conditions: Hernia, Ventral, Hernia, Abdominal, Hernia Abdominal Wall