Lateral Epicondylitis Clinical Trial
Official title:
Safety and Effects of PDRN(Polydeoxyribonucleotide) Injection in Patient With Elbow Epicondylitis in Randomized Double-blind Active-control Comparative Study
This study is to assess the safety and effect of polydeoxyribonucleotide(PDRN) on the
lateral epicondylitis with ultrasonography-guided injection of the PDRN or dextrose
solution.
Condition: lateral epicondylitis
Intervention Drug: polydeoxyribonucleotide, PDRN Drug: dextrose solution, 15% as
prolotherapy, active control
Phase 4
Study type: Interventional
Study design: Treatment, Parallel Assignment, Double Blind((Subject, intervention performer,
Investigator, Outcomes Assessor), Randomized, Safety/Efficacy Study
Official Title: Safety and Effects of PDRN(polydeoxyribonucleotide) Injection in Patient
with elbow epicondylitis in randomized double-blind active-control comparative study
Estimated Enrollment: 40
Detailed Description:
40 patients that meet the inclusion criteria on screening test are assigned to one of two
groups(PDRN group or 15% dextrose active control group) by randomization. They take the
three times of the ultrasonography-guided injections for four weeks(0,2,4 weeks) under
double-blind. PDRN group take ultrasonography-guided 3ml PDRN injection for the lesion( tear
or tendinosis about extensor carpi radialis brevis, extensor digitorum communis, radial
collateral ligament ) of lateral epicondylitis for 4 weeks. Active control group takes the
15% dextrose solution, 3ml for same procedure. The main outcome variables are measured at 0,
6 weeks and 3 months after 1st injection as starting point and compared differences from
baseline to 3 month as primary end points within each group or between both group.
Polydeoxyribonucleotide is verified whether it has the safety and effect on lateral
epicondylitis with comparing to prolotherapy.
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