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NCT04947202: SAFIL_MESH
Clinical Study on the Safety of SAFIL® MESH
trial testing Hernioplasty in Abdominal Wall Defect in 152 participants. Completed in 30 November 2021.
30 November 2021
Quick facts
| Lead sponsor | Aesculap AG |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 152 |
| Start date | 1 July 2021 |
| Primary completion | 30 November 2021 |
| Estimated completion | 30 November 2021 |
| Sites | 2 locations across Spain |
Drugs / interventions tested
- Hernioplasty
Conditions studied
- Abdominal Wall Defect — all drugs for Abdominal Wall Defect →
- Ventral Hernia — all drugs for Ventral Hernia →
- Abdominal Hernia — all drugs for Abdominal Hernia →
- Fascial Hernia — all drugs for Fascial Hernia →
Sponsor
Aesculap AG — full company profile →
Who can join
Eligibility, any sex, with Abdominal Wall Defect or Ventral Hernia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Observational, Retrospective, Multi-center Clinical Study on the Safety of SAFIL® MESH in Patients Undergoing Reinforcement of Soft Tissues After Abdominal Wall Surgery or Other Fascial Defects
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04947202
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Abdominal Wall Defect
Currently open trials in the same condition.
- NCT06367309 — ExtrAperitoneaL Plasty vs Intraperitoneal oNlay mEsh in Ventral Hernia Repair · NA · recruiting
- NCT03310905 — Abdominal Wall Transplant · NA · recruiting
Other Aesculap AG trials
Trials by the same sponsor.
- NCT05441618 — Post Market Clinical Follow-Up Study on the Performance and Safety of Lyoplant® · completed
- NCT05944081 — Postmarket Clinical Follow-Up Study on Arcadius XP L® Interbody Fusion Device · withdrawn
- NCT06298500 — Clinical Performance of HISTOACRYL® LAPFIX - CANNULA for Laparoscopic Inguinal Hernia Repair · completed
- NCT06055946 — Symmcora® Long-term Bidirectional Barbed Suture for Anastomosis in Patients Undergoing Robot Assisted Radical Prostatect · completed
- NCT05182320 — Study Measuring the Effects of Patient Data for Total Hip and Total Knee Arthroplasty Patients Using an APP Based Sensor · withdrawn
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 NCT04947202 (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 Aesculap AG
- Last refreshed: 24 January 2022
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/NCT04947202.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing