Evaluating functional status in patients with Achilles tendon rupture
Functional Status for Surgically and Non-surgically Treated Patients With Acute Achilles Tendon Rupture Following a Public Municipal Rehabilitation - A Prospective Cohort Study
This study looks at how well people aged 18 and older recover from an Achilles tendon rupture by comparing those who had surgery to those who didn't, using tests to measure their strength and endurance.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Københavns Kommune Academic / other |
| Locations | 2 sites (Copenhagen N. and 1 other locations) |
| Trial ID | NCT06602908 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the functional status of patients who have experienced an acute Achilles tendon rupture, comparing outcomes between those treated surgically and non-surgically. The study focuses on patients aged 18 and older who have consented to participate and were treated within 14 days of their injury. Functional outcomes will be measured using heel rise tests to evaluate endurance and maximum heel rise height. The study is conducted in rehabilitation centers in Copenhagen, Denmark.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older with an acute Achilles tendon rupture treated within 14 days of injury.
Not a fit: Patients with bilateral Achilles tendon ruptures or those experiencing a re-rupture of a previous Achilles tendon injury may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into the best rehabilitation practices for improving functional outcomes in patients with Achilles tendon ruptures.
How similar studies have performed: Other studies have explored rehabilitation protocols for Achilles tendon ruptures, but this specific observational approach is less common.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient has an acute achilles tendon rupture (treated within 14 days after injury). * Adult patients aged of 18 years or older. * Patients has given informed consent to participate in the study. Exclusion Criteria: * Patients with bilateral achilles tendon rupture * Patients with re-rupture of previous achilles tendon rupture
Where this trial is running
Copenhagen N. and 1 other locations
- Centre of rehabilitation Nørrebro — Copenhagen N., Denmark (Recruiting)
- Centre of rehabilitation Vanløse — Vanløse, Denmark (Recruiting)
Study contacts
- Study coordinator: Jonas Samsø Larsen, Cand. Scient. Phys.
- Email: au19@kk.dk
- Phone: 0045+24493133
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.