PhaseII Study of SI-657 in Patients with Enthesopathy (Lateral Epicondylitis)

Authors
Category Primary study
Registry of TrialsUMIN Clinical Trials Registry
Year 2012
INTERVENTION: Placebo group SI‐657 group CONDITION: Enthesopathy (Lateral Epicondylitis) PRIMARY OUTCOME: Efficacy Outcome;; Change of Visual Analogue Scale (VAS) of pain at final evaluation. SECONDARY OUTCOME: Efficacy Outcomes;; Roles and Maudsley score; ; Safety Outcomes;; Adverse events; Laboratory tests INCLUSION CRITERIA: 1.Patients diagnosed with lateral epicondylitis 2.Patients with 12 weeks or longer symptoms 3.Patients between 20 and 75 years old.
Epistemonikos ID: 7b1aece901af2fd9eefd629f2e45040cc08987f2
First added on: Aug 22, 2024