Last reviewed · How we verify

NCT06990100: DT4-EBMCA

Clinical Performance and Safety of ENDOPACK® DT4-EBMCA in ACL Reconstruction 24 Months Post-surgery : Post-market Clinical Follow-up Study

Completed NA Last updated 25 May 2025
What this trial tests

NA trial testing ACL surgery in ACL Rupture in 36 participants. Completed in 12 May 2025.

Timeline
1 October 2024
Primary endpoint
1 April 2025
12 May 2025

Quick facts

Lead sponsorSACIMEX
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment36
Start date1 October 2024
Primary completion1 April 2025
Estimated completion12 May 2025
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

SACIMEX

Who can join

18 and older, any sex, with ACL Rupture. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Anterior cruciate ligament (ACL) injuries are among the most common sports-related knee traumas. The DT4-EBMCA device, based on a quadrupled semitendinosus autograft technique, aims to provide effective and minimally invasive ligament reconstruction. This study evaluates its long-term performance and safety in routine clinical practice.

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:

Verify against primary sources

Data sources for this page

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/NCT06990100.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing