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NCT06601088: C-NMES-ATR

Achilles Tendon Rupture - Intervention With Electrical Stimulation

Not yet recruiting NA Last updated 19 September 2024
What this trial tests

NA trial testing Neuromuscular Electrical Stimulation in Achilles Tendon Ruptures in 220 participants. Not yet recruiting.

Timeline
15 January 2025
Primary endpoint
15 February 2026
30 December 2026

Quick facts

Lead sponsorKarolinska University Hospital
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment220
Start date15 January 2025
Primary completion15 February 2026
Estimated completion30 December 2026

Drugs / interventions tested

Conditions studied

Sponsor

Karolinska University Hospital

Who can join

Adults 18 to 75, any sex, with Achilles Tendon Ruptures or Immobilization. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Acute Achilles tendon rupture (ATR) is an injury that is commonly associated with complications, such as blood clotting, muscle loss and tendon lengthening, all of which affect the long-term outcome and return to sports. These complication are related to the treatment of ATR with lower leg immobilization in a boot. The investigators aim to demonstrate that an intervention with calf neuromuscular electrical stimulation (C-NMES) during leg immobilization after ATR can 1) reduce blood clots, 2) lower the degree of muscle loss, 3) decrease tendon lengthening and 4) improve long-term outcome.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Neuromuscular Electrical Stimulation

Trials testing the same drug.

Other recruiting trials for Achilles Tendon Ruptures

Currently open trials in the same condition.

Other Karolinska University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06601088.

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