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NCT05734222
Optimization of Surgical Treatment of Patients With Incisional Ventral Hernias
NA trial testing A new method of repair of the abdominal wall of mid-lateral postoperative ventral hernias in Hernia, Ventral in 110 participants. Currently enrolling.
30 April 2025
Quick facts
| Lead sponsor | Samara State Medical University |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | crossover |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 110 |
| Start date | 29 September 2022 |
| Primary completion | 30 April 2025 |
| Estimated completion | 23 May 2025 |
| Sites | 1 location across Russia |
Drugs / interventions tested
- A new method of repair of the abdominal wall of mid-lateral postoperative ventral hernias
Conditions studied
- Hernia, Ventral — all drugs for Hernia, Ventral →
- Hernias Intestinal — all drugs for Hernias Intestinal →
- Hernia Abdominal Wall — all drugs for Hernia Abdominal Wall →
Sponsor
Samara State Medical University
Who can join
Adults 25 to 88, any sex, with Hernia, Ventral or Hernias Intestinal. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of our work of optimization of the treatment of postoperative hernias is to improve the results of treatment of patients with median and median-lateral postoperative hernias of medium (W2) and large (W3) sizes by developing new surgical techniques. The main questions it aims to answer are: 1. To study the topographic and variant anatomy of vessels and nerves in the retromuscular, preperitoneal, postperitoneal and pre-abdominal cell spaces of the anterior abdominal wall. To determine the most probable sources of blood flow and lymph from the anatomical formations forming the bed of the endoprosthesis. 2. To develop technical, surgical techniques that allow to form an implant bed with minimal traumatization of blood vessels and nerves and reduce the risk of postoperative complications. 3. To develop a technique for plasty of the anterior abdominal wall in mid-lateral postoperative hernias with a combination of retromuscular and subaponeurotic spaces. The researchers will compare an experimental group in which a new method of preparing the implant place will be used and a control group in which standard methods of treating postoperative ventral hernias were used to see whether the new method affects the improvement of the postoperative period and the reduction of complications.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05734222
- 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
- NCT06051578 — Abdominal Wall Tension in Patients Undergoing Ventral Hernia Repair Without Component Separation · active not recruiting
- NCT05094089 — Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application · active not recruiting
- NCT04779918 — Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh · NA · recruiting
Other Samara State Medical University trials
Trials by the same sponsor.
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- NCT05802849 — Acetazolamide Per os for Decompensation of Heart Failure · Phase 4 · recruiting
- NCT05736159 — Scientific Justification of Assessment Criteria and Improvement of the Methodology for Assessing School Maturity · active not recruiting
- NCT05817006 — Research of the Long-COVID-19 Syndrome in the Children · NA · completed
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 NCT05734222 (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 Samara State Medical University
- Last refreshed: 1 January 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/NCT05734222.
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