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Effect of Jiuwei Zhuhuang Powder on Cough Resolution in Children with Upper Respiratory Tract Infections: A Multicenter Randomized Controlled Trial.
Luo, Hui; Song, Gui-Hua; Ma, Xiao-Jian; Sun, Meng-Meng; Zhang, Man; Xie, Jian-Rong; Peng, Shao.
Afiliação
  • Luo H; Institute for Tibetan Medicine, China Tibetology Research Center, Beijing, 100101, China.
  • Song GH; Department of Pediatrics, the First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, 450000, China.
  • Ma XJ; Department of Pediatrics, Huaihe Hospital of Henan University, Zhengzhou, 450000, China.
  • Sun MM; Department of Pediatrics, the First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, 450000, China.
  • Zhang M; Department of Pediatrics, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, 475000, China.
  • Xie JR; School of Statistics, Renmin University of China, Beijing, 100872, China.
  • Peng S; Department of Pediatrics, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, 475000, China. Pengshaodh630@126.com.
Chin J Integr Med ; 28(5): 387-393, 2022 May.
Article em En | MEDLINE | ID: mdl-34913149
ABSTRACT

OBJECTIVE:

To assess the effectiveness of Jiuwei Zhuhuang Powder (JWZH), a Tibetan patent medicine in treating upper respiratory tract infection (URTI) associated cough in children.

METHODS:

The study was a multicenter, randomized, open-label, controlled trial. A total of 142 children aged 2 to 14 years old, with URTI-associated cough within 48 h of onset, were randomly assigned to two groups at a 11 ratio by computer-generated randomization sequence. Children were treated with JWZH (1 to 1.5 g, twice to thrice daily) in the treatment group or conventional treatment (Pediatric Paracetamol, Artificial Cow-bezoar and Chlorphenamine Maleate Granules, 0.25 to 1 g, thrice daily) in the control group for 5 days. The primary endpoints were the time to cough resolution and 4-day cough resolution rate. The secondary endpoints were the daily improvement in symptom scores and cough resolution rate during the study period.

RESULTS:

A total of 138 children were included in the intention-to-treat analysis, with 71 cases in the treatment group and 67 cases in the control group. Compared with the conventional treatment, the children receiving JWZH had a shorter time to cough resolution [hazard ratio, 2.10; 95% confidence interval (CI), 1.29-3.40; P=0.003]. The median time to cough resolution for children receiving JWZH was shorter than that of the conventional treatment (2 days vs. 3 days; P<0.001). The 4-day cough resolution rate in the JWZH group was higher than that of the control group (94.4% vs. 74.6%; risk difference 19.8%, 95% CI 8.1%-31.5%; relative risk 1.265, 95% CI 1.088-1.470; P=0.001). There were no statistically significant differences in the improvement of other symptoms caused by URTI (P>0.05). Adverse events was reported in 5.6% (4/71) and 4.5% (3/67) in participants of JWZH and PPACCM groups (P>0.05), respectively, which were all mild and resolved without treatment.

CONCLUSION:

JWZH seemed to be a safe and effective therapy for URTI-associated cough in children. (Trial registration No. ChiCTR2000039421).
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Texto completo: 1 Base de dados: MEDLINE Medicinas Tradicionais: Medicinas_tradicionales_de_asia / Medicina_china / Medicina_tibetana Assunto principal: Infecções Respiratórias / Tosse Tipo de estudo: Clinical_trials / Etiology_studies Idioma: En Revista: Chin J Integr Med Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Medicinas Tradicionais: Medicinas_tradicionales_de_asia / Medicina_china / Medicina_tibetana Assunto principal: Infecções Respiratórias / Tosse Tipo de estudo: Clinical_trials / Etiology_studies Idioma: En Revista: Chin J Integr Med Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China