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NCT06051578
Abdominal Wall Tension in Patients Undergoing Ventral Hernia Repair Without Component Separation
trial testing Abdominal wall tension measurement in Hernia, Ventral in 50 participants. Participants enrolled and being followed up; not accepting new ones.
22 May 2025
Quick facts
| Lead sponsor | The Cleveland Clinic |
|---|---|
| Status | Active, enrolled |
| Study type | OBSERVATIONAL |
| Enrollment | 50 |
| Start date | 8 September 2023 |
| Primary completion | 22 May 2025 |
| Estimated completion | 1 May 2026 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Abdominal wall tension measurement
Conditions studied
- Hernia, Ventral — all drugs for Hernia, Ventral →
- Hernia, Abdominal — all drugs for Hernia, Abdominal →
- Hernia Abdominal Wall — all drugs for Hernia Abdominal Wall →
Sponsor
The Cleveland Clinic
Who can join
18 and older, any sex, with Hernia, Ventral or Hernia, Abdominal. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to use a scale to learn more about the tension of the abdominal wall in hernia repairs without component separation. 1. What is the abdominal wall tension for hernias repaired without a component separation? 2. What patient factors contribute to greater abdominal wall tension? 3. Is there an association between abdominal wall tension before primary closure or bridging repair and patient outcomes? Participants will be asked to allow their surgeon to use a tension scale to measure the tension of the abdominal wall during surgery.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06051578
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Hernia, Ventral
Currently open trials in the same condition.
- NCT07316426 — Preoptimisation in Ventral Hernia Surgery · NA · recruiting
- NCT06449378 — Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open Repair of Ventral Hernia · NA · active not recruiting
- NCT05094089 — Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application · active not recruiting
- NCT05734222 — Optimization of Surgical Treatment of Patients With Incisional Ventral Hernias · NA · recruiting
- NCT04779918 — Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh · NA · recruiting
Other The Cleveland Clinic trials
Trials by the same sponsor.
- NCT07218198 — Clinical Decision Support Tool for the Treatment of Uncontrolled Hypertension · NA · not yet recruiting
- NCT07442747 — Neural Mechanisms of Aerobic Exercise Benefits in PD With DBS · NA · not yet recruiting
- NCT07471464 — Centered Surgery - Preoperative Counseling and Patient Satisfaction · recruiting
- NCT07073963 — Virtual Patient Groups for Sarcoidosis Associated Fatigue · NA · recruiting
- NCT07363343 — Nifedipine and Enalapril vs Nifedipine and Labetalol for the Treatment of Postpartum Hypertension Study · NA · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06051578 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by The Cleveland Clinic
- Last refreshed: 3 December 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06051578.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing