Status:
UNKNOWN
Outcome After Surgical Reconstruction of the Achilles Tendon Insertion.
Lead Sponsor:
Krankenhaus Barmherzige Schwestern Linz
Conditions:
Achilles Tendinopathy
Insertional Achilles Tendinopathy
Eligibility:
All Genders
18+ years
Brief Summary
The purpose of this study is to evaluate the functional outcomes and sports ability after surgical treatment of insertional Achilles tendon tendinopathy using tendon detachment, debridement, and doubl...
Detailed Description
The lifetime risk of Achilles tendon pain is approximately 6%, one-third of whom complain of pain at the bony attachment of the Achilles tendon to the calcaneus. Primary treatment of these insertiona...
Eligibility Criteria
Inclusion
- All patients who underwent reconstruction and double-row anchor refixation of the Achilles tendon insertion due to an insertional tendinopathy of the Achilles tendon.
Exclusion
- Lack of informed consent
- Revision surgery
- Patients who had another operation on the same leg during the same procedure or 6 months later
Key Trial Info
Start Date :
September 13 2022
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 1 2024
Estimated Enrollment :
23 Patients enrolled
Trial Details
Trial ID
NCT06030908
Start Date
September 13 2022
End Date
October 1 2024
Last Update
November 29 2023
Active Locations (1)
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1
Ordensklinikum Linz, Barmherzige Schwestern Abteilung Orthopädie
Linz, Austria, 4010