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NCT04793971 Clinical Trial

Minimal Invasive Treatment of Achilles Tendinopathy: Focus on Percutaneous Release (Maffulli)

Tendinopathy Clinical Trial

Official title:
Minimal Invasive Treatment of Achilles Tendinopathy: Focus on Percutaneous Release (Maffulli)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04793971
Other study ID # S57392
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 2014
Est. completion date April 2015

Study information
Verified date March 2021
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To evaluate the outcome of percutaneous paratenon release for chronic midportion Achilles tendinopathy.

Description:

Since 2011 the percutaneous procedure took the place of the open release of the paratenon for the surgical treatment for chronic midportion Achilles tendinopathy in the investigators' center. In this study the investigators re-evaluate the patients undergoing percutaneous surgery since then in order to compare the outcome with the excellent results cited in literature. The patients will be contacted and asked to participate completing a VAS-score, a VISA-A score and agreeing with a clinical examination. Approving by the Ethical Committee of UZLeuven is pending.

Recruitment information / eligibility
Status Completed
Enrollment 8
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - patients that underwent percutaneous paratenon release for chronic midportion Achilles tendinopathy Exclusion Criteria: - insertional tendinopathy - open intervention - (partial) Achilles tendon rupture

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• percutaneous paratenon release
percutaneous paratenon release for chronic midportion Achilles tendinopathy

Locations
Country Name City State
Belgium University Hospitals of Leuven Pellenberg Vlaams-Brabant

Sponsors (1)
Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary VISA-A-score specific questionnaire about (mal-)function of Achilles tendon 3 months
Secondary SF-36-score questionnaire about well-being 3 months
Secondary VAS-score questionnaire about pain 3 months
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