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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04793971
Enrollment
8
Registered
2021-03-11
Start date
2014-11-30
Completion date
2015-04-30
Last updated
2021-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tendinopathy

Keywords

chronic midportion Achilles tendinopathy, percutaneous paratenon release

Brief summary

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

Detailed 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.

Interventions

PROCEDUREpercutaneous paratenon release

percutaneous paratenon release for chronic midportion Achilles tendinopathy

Sponsors

Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients that underwent percutaneous paratenon release for chronic midportion Achilles tendinopathy

Exclusion criteria

* insertional tendinopathy * open intervention * (partial) Achilles tendon rupture

Design outcomes

Primary

MeasureTime frameDescription
VISA-A-score3 monthsspecific questionnaire about (mal-)function of Achilles tendon

Secondary

MeasureTime frameDescription
SF-36-score3 monthsquestionnaire about well-being
VAS-score3 monthsquestionnaire about pain

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026