Achilles Injuries Tendon

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Review clinical trials related to Achilles Injuries Tendon. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Blood Flow Restriction Therapy in Achilles Injury

Blood flow restriction (BFR) therapy is a brief and partial restriction of venous outflow of an extremity during low load resistance exercises. It is a safe and effective method of improving strength in healthy and active individuals, recovering from orthopedic pathologies and procedures. This prospective, randomized study will look at the implications this form of treatment has on the rehabilitation of Achilles injuries.

Participants needed: 57
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

Diagnosed with Achilles Injury [+2]

Patients with intention to receive standard therapy and not the study therapy [+4]

Status: Not yet recruiting

Extracorporeal Shockwave Therapy and Platelet-Rich Plasma for Midportion Achilles Tendinopathy

Midportion Achilles tendinopathy is a common cause of pain and functional limitation in both athletes and the general population. Progressive tendon loading programs are considered first-line treatment but do not lead to satisfactory outcomes in all patients. Extracorporeal shockwave therapy (ESWT) and platelet-rich plasma (PRP) injections are commonly used interventions for refractory symptoms, yet evidence supporting their combined use is limited particularly in treating Achilles tendon disorders. This randomized controlled trial will evaluate the effectiveness of a standardized exercise program alone or in combination with PRP injection, ESWT, or both therapies in active adults with midportion Achilles tendinopathy. Participants will be randomized to one of four treatment groups and followed for six months. The primary outcome will assess changes in Achilles tendon symptoms and function using the Victorian Institute of Sport Assessment-Achilles (VISA-A) score. Secondary outcomes will include patient-reported outcomes, physical function testing, ultrasound tendon structure measures, and gait biomechanics.

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Spaulding Rehabilitation HospitalUpdated: May 13, 2026Locations: 1
Eligibility criteria

Age 18-65 years [+5]

Symptoms present for less than 3 months [+9]

Status: Recruiting

French Achilles Tendon Surgery Cohort Study

This 20-year prospective cohort study monitors patients following Achilles tendon repair to assess re-rupture rates, long-term functional outcomes, return-to-sport rates, and procedure-related complications. The aim is to better understand the long-term durability and clinical effectiveness of Achilles tendon repair techniques to optimize patient outcomes.

Participants needed: 5,000
Trial details
Age: 7+Biological sex: AllType: ObservationalSponsor: Chirurgie Du SportUpdated: Mar 19, 2026Locations: 1Duration: 20 Years
Eligibility criteria

Patients undergoing Achilles tendon repair surgery

Patient refusal