This study is a multicenter, randomized, double-blind, placebo-controlled clinical trial to evaluate the efficacy and safety of Yuxuebi tablet in treating night pain of Ankylosing Spondylitis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
60
0.5g/ tablet
0.5g/ tablet
Guang'anmen Hospital
Beijing, China
The First People's Hospital of Guangzhou
Guangzhou, China
The First People's Hospital of Jinzhong
Jinzhong, China
Nanchong Central Hospital
Nanchong, China
Change in Visual analogue scale (VAS) for night pain
Time frame: Baseline, at day 7, day 14, day 28, day 42 during treatment
Visual analogue scale (VAS) for whole day
Time frame: Baseline, at day 7, day 14, day 28, day 42 during treatment
BASDAI (Bath Ankylosing Spondylitis Disease Activity Index)
Time frame: Baseline, at day 28, day 42 during treatment
BASFI (Bath Ankylosing Spondylitis Functional Index)
Time frame: Baseline, at day 28, day 42 during treatment
BASMI (Bath Ankylosing Spondylitis Metrology Index)
Time frame: Baseline, at day 28, day 42 during treatment
Syndrome score of traditional Chinese medicine
The Evaluation Scale of Syndrome score ranges from 0 (best score) to 15 (worst score).
Time frame: Baseline, at day 28, day 42 during treatment
SF-36 (The Medical Outcomes Study 36-item short-form health survey)
Time frame: Baseline, at day 42 during treatment
ESR (Erythrocyte Sedimentation Rate)
Time frame: Baseline, at day 14, day 28, day 42 during treatment
CRP (C-Reactive Protein)
Time frame: Baseline, at day 14, day 28, day 42 during treatment
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Shenzhen Traditional Chinese Medicine Hospital
Shenzhen, China