Huaiqihuang Granule Improves Bleeding in Childhood CITP: 71.74% Effectiveness vs 45.65% Placebo
This multi-centre, randomized, double-blind, placebo-controlled clinical trial evaluated the efficacy and safety of Huaiqihuang Granule (HQH) in 216 children with chronic immune thrombocytopenia (CITP) across 13 hospitals in China. Participants were randomized to receive either HQH or placebo for a 24-week double-blind period, followed by a 24-week open-label period where placebo recipients switched to HQH. The primary endpoint was the clinical effectiveness rate, defined by a decrease in bleeding grade and platelet response. HQH demonstrated a significantly higher clinical effectiveness rate of 71.74% compared to 45.65% in the placebo group (p=0.0013). This result remained consistent even when patients requiring rescue treatment were considered ineffective or excluded. Secondary endpoints included safety assessments, where adverse events (AEs) and serious AEs were comparable between groups. Notable severe AEs were thrombocytopenia (6.9%), respiratory tract infection (5.1%), and hemorrhagic episodes (2.8%). The study concludes that HQH is effective in improving bleeding outcomes in children with CITP and maintains a favorable safety profile over long-term use. These findings suggest HQH as a viable treatment option for pediatric CITP, warranting consideration in clinical practice.