PMCF Study of the AchilloCordPLUS System Implant Set for Acute Achilles Tendon Repair
NCT05304819 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 19
Last updated 2026-04-21
Summary
This is a Post Market Clinical Follow Up Study in Orthopaedics, it will verify the long-term safety and performance of the device in the intended patient population, when indicated for the acute repair of the Achilles tendon.
The Medical Device in this study AchilloCordPLUS is a Class IIb UKCA-Marked device manufactured by Xiros Ltd.
Conditions
- Achilles Tendon Rupture
Interventions
- DEVICE
-
AchilloCordPLUS™ System Implant
AchilloCordPLUS System Implant Set for Acute Achilles Tendon Repair
Sponsors & Collaborators
-
Xiros Ltd
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-03-09
- Primary Completion
- 2026-01-31
- Completion
- 2026-01-31
Countries
- United Kingdom
Study Locations
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