Achilles Tendon Injury

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

Condition / disease
Location
Status: Not yet recruiting

Morphological and Mechanical Assessment in the Achilles Tendon After Radiofrequency Stimulation in Runners

448 kHz capacitive-resistive monopolar radiofrequency is an emerging physiotherapy technique whose usefulness and clinical relevance still need to be investigated. This study is a pre-post quasi-experimental study in which several variables will be measured before and immediately after 448 kHz capacitive resistive monopolar radiofrequency. It aims to analyze the morphological and mechanical changes in the Achilles tendon following the intervention in healthy runners.

Participants needed: 19
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University of MalagaUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Adults aged 18-65 [+2]

History of lower limb surgery, rheumatic or neuromuscular diseases or pregnancy [+2]

Status: Recruiting

Assessment of Medrol Dosepak to Reduce Opioid Consumption in Foot and Ankle Surgical Patients

This clinical trial aims to determine the effects of a 6-day low-dose methylprednisolone course on pain, nausea, and total opioid consumption in patients undergoing foot and ankle surgeries. The secondary objective of the study is to determine and monitor the effects of the course on complications following surgery and patient-reported outcomes

Participants needed: 180
Trial details
Phase: Phase 2Age: 18-95Biological sex: AllType: InterventionalSponsor: Emory UniversityUpdated: Mar 9, 2026Locations: 2
Eligibility criteria

Concurrent or significant injuries to other bones or organs [+7]

Status: Not yet recruiting

CUHK Achilles Tendon Disorder Registry

This is a long-term research registry for patients with Achilles tendon disorders (like tears, chronic pain, or ruptures) as well as healthy adults without tendon problems. The goal is to collect detailed information over time to understand which treatments work best for different people, identify risk factors for injury, and improve overall care. Adults over 18, both with and without Achilles tendon conditions, are eligible to join. Participants will attend several assessment visits at the Prince of Wales Hospital over the first year (at the start, 6 weeks, 3, 4, 6, and 12 months) for physical tests, ultrasounds, and questionnaires. After the first year, follow-up continues with annual online questionnaires for up to five years. The main measure is a standard questionnaire about tendon pain and function (VISA-A). The study aims to use this information to guide better, more personalized rehabilitation strategies, improve patient outcomes, and reduce long-term disability. All participation is voluntary and requires written consent.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Chinese University of Hong KongUpdated: Jan 9, 2026Duration: 5 Years
Eligibility criteria

Adults (>18 years of age)

Any physical or psychological comorbidity that would impair the ability to compl... [+1]