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ABSTRACT: Objective
To evaluate the efficacy and safety of Chuanxiong Qingnao Granule (CQG) to treat migraine.Method
This study was a randomized, double-blind, placebo-controlled trial. All migraineurs were recruited and randomly assigned into a treatment group treated with CQG and a control group treated with a placebo. The whole research process included a 4-week baseline, 12-week intervention, and 12-week follow-up. The primary outcome was responder rate, defined as the percentage of migraineurs with 50% or more reduction in the frequency of migraine attack during treatment and posttreatment period compared with the baseline. The secondary outcomes were the number of migraine days, migraine attack frequency, visual analogue scale (VAS), Fatigue Severity Scale (FSS), Hamilton Depre
SUBMITTER: Li YF
PROVIDER: S-EPMC8716194 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature