Efficacy of Percutaneous Electrolysis in the Treatment of Achilles Tendinopathy
Evaluation of the Efficacy of Adding Low-intensity Percutaneous Musculoskeletal Electrolysis to the Conservative Treatment of Noninsertional Achilles Tendinopathy: a Randomized Controlled Clinical Trial
Sponsor: Maimonides University
Listed as NCT05301959, this observational or N/A phase trial focuses on Achilles Tendinopathy and remains actively recruiting participants. Sponsored by Maimonides University, it has been updated 10 times since 2023, reflecting substantial change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.
Status Flow
Change History
10 versions recorded-
May 4, 2026 — Present [daily]
Recruiting
Status: Unknown → Recruiting · Phase: NA → None
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Feb 2026 — May 2026 [monthly]
Unknown NA
Status: Recruiting → Unknown
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Sep 2025 — Feb 2026 [monthly]
Recruiting NA
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Sep 2024 — Sep 2025 [monthly]
Recruiting NA
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Jul 2024 — Sep 2024 [monthly]
Recruiting NA
▶ Show 5 earlier versions
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Sep 2023 — Jul 2024 [monthly]
Recruiting NA
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Jun 2023 — Sep 2023 [monthly]
Recruiting NA
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Sep 2022 — Jun 2023 [monthly]
Recruiting NA
Status: Not Yet Recruiting → Recruiting
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May 2022 — Sep 2022 [monthly]
Not Yet Recruiting NA
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Apr 2022 — May 2022 [monthly]
Not Yet Recruiting NA
First recorded
Eligibility Summary
Achilles tendinopathy (AT) is one of the most reported myotendinous pathologies due to overuse in the literature. In the general adult population, its incidence is 2.35 cases per 1,000 patients, with no difference between men and women. The international literature reports that up to 29% of patients fail with conservative treatment. Within physiotherapy, new alternatives for the treatment of tendinopathies arise, applying electric currents percutaneously, which from a mechanical effect associated to the use of a needle and an electric effect by the use of galvanic currents, generate a local inflammatory response; activation of the central nervous system and analgesia. The aim of the research is to evaluate the efficacy of adding low intensity percutaneous electrolysis to the treatment with a high load eccentric exercise program based on the protocol of Silbernagel et al. in adults with Achilles tendinopathy to improve its functionality. A randomized, double-blind, blinded, evaluator-blinded, controlled clinical trial will be conducted in parallel groups (experimental treatment vs. sham treatment), with a follow-up at 26 and 52 weeks after the first intervention. Non-probability and intentional sampling will be performed.
Contact Information
- Maimonides University
For direct contact, visit the study record on ClinicalTrials.gov .