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ACTIVE NOT RECRUITING
NCT05304819

PMCF Study of the AchilloCordPLUS System Implant Set for Acute Achilles Tendon Repair

Sponsor: Xiros Ltd

View on ClinicalTrials.gov

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.

Official title: Post-market Clinical Follow-up (PMCF) Study of the AchilloCordPLUS System Implant Set for Acute Achilles Tendon Repair

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

19

Start Date

2022-03-09

Completion Date

2026-01

Last Updated

2025-01-31

Healthy Volunteers

No

Interventions

DEVICE

AchilloCordPLUS™ System Implant

AchilloCordPLUS System Implant Set for Acute Achilles Tendon Repair

Locations (1)

North Cumbria Integrated Care Nhs Foundation Trust

Penrith, United Kingdom