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Clinical Trial Summary

Study purpose is to evaluate the effectiveness of Platelet-rich Plasma (PRP) injection in the treatment of trigger finger. We compare PRP to a corticosteroid (methylprednisolone) injection in a prospective randomized triple-blind placebo-controlled study. Patients with clinically confirmed trigger finger are randomized (1:1:1 computer generated sequence with random block size) to three parallel groups and will receive an injection of either PRP, corticosteroid or placebo (0.9% saline) around the affected tendon sheath in a double-blind setting. Baseline data is collected and is followed by a phone call at 1 month, and follow-up visits at 3, 6, 12 and 24 months after the intervention. Unveiling of the allocation is at 6 months post-intervention. The primary outcome measures are: - Symptom resolution - Patient-Rated Wrist Evaluation Secondary outcomes: - Quick-Disabilities of the Arm, Shoulder and Hand - Pain Visual Analogue Score - Global improvement (7-step Likert-scale) - Grip strength - Finger range of motion


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04167098
Study type Interventional
Source Töölö Hospital
Contact Samuli Aspinen, M.D., Ph.D
Phone +358406360546
Email samuli.aspinen@hus.fi
Status Recruiting
Phase N/A
Start date November 1, 2019
Completion date July 1, 2022