UnknownNot Applicable

Outcome After Surgical Reconstruction of the Achilles Tendon Insertion.

Austria23 participantsStarted 2022-09-13

Plain-language 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 double-row anchor refixation.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 Criteria: * Lack of informed consent * Revision surgery * Patients who had another operation on the same leg during the same procedure or 6 months later

What they're measuring

Return to sports Rate

Timeframe: minimum 12 months from surgery to follow-up

Trial details

NCT IDNCT06030908

SponsorKrankenhaus Barmherzige Schwestern Linz

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-10

View on ClinicalTrials.gov More Achilles Tendinopathy trials