The purpose of this study is to evaluate the Efficacy and Safety of Smilon® in the Depression Patients with pain. Eligible patients will be randomly assigned to 1 of 2 arms, either Smilon® or placebo, and will receive the treatment for 8 weeks in this study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
30
Nang Kuang Pharmaceutical Co., LTD
Tainan, Xinhua Township, Taiwan
Evaluation of pain intensity using the visual analog scale (VAS)
Time frame: 8-week treatment
Evaluation of Severity of depressive symptom using the Depression and Somatic Symptoms Scale (DSSS)
Time frame: 8-week treatment
Evaluation of Severity of depressive and anxious symptom using the Hamilton depression scale (HAM-D) and Hamilton anxiety scale (HAM-A)
Time frame: 8-week treatment
Evaluation of quality of life assessed by a 28-item WHOQoL self-administered questionnaire
Time frame: 8-week treatment
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