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Plantaris Friction Syndrome clinical trials

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NCT ID: NCT03077009 Recruiting - Clinical trials for Non-Insertional Achilles Tendinopathy

Functional Improvement and UTC of the Achilles Tendon After Sodium Hyaluronate Injection for Plantaris Syndrome

Start date: March 20, 2017
Phase: Phase 4
Study type: Interventional

This is a study to assess the benefit of sodium hyaluronate (Ostenil) injection for plantaris friction syndrome (PFS) associated with midportion Achilles tendinopathy. Functional outcome scores will be recorded prior to treatment and at regular intervals up to 2 years. Changes in tendon structure will be assessed using ultrasonographic tissue characterisation (UTC). UTC will be performed prior to treatment and also at regular intervals up to 6 months following injection.