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Study identifier: NCT07650396 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

The ASPIRE Trial: AchilleS tendinoPathy Treated With cortIcosteRoid injEctions

Condition: Achilles Tendinopathy (AT)  ·  Sponsor: Erasmus Medical Center

PhasePhase 3
Planned participants276
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

Achilles tendinopathy is a common and often persistent tendon disorder associated with pain, impaired function, and reduced participation in physical activities. Standard care consists of education, load management advice, and progressive calf-strengthening exercises, yet about half of patients remain symptomatic. Corticosteroid injections are frequently used in clinical practice, but evidence on long-term efficacy and safety remains inconclusive. The ASPIRE trial is a multicentre, randomized, double-blind, placebo-controlled phase III trial evaluating whether 1-3 ultrasound-guided peritendinous corticosteroid injections added to standard care are safe and more effective than placebo injections plus standard care in adults with chronic midportion Achilles tendinopathy. The primary outcomes are change in VISA-A score over 1 year and incidence of full-thickness Achilles tendon rupture during 1-year follow-up.

This description comes directly from the study's public registry record.

Talk to the study team

Kristel van Abswoude, MD  ·  +31 6 49326353  ·  aspire@erasmusmc.nl

Always discuss trial participation with your own doctor first.

Locations (1)

Erasmus MCRotterdam, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT07650396