Effectiveness and Safety of Chinese Medicine to Treat Hand, Foot, and Mouth Disease

Sponsor
Jiangxi Qingfeng Pharmaceutical Co. Ltd. (Industry)
Overall Status
Completed
CT.gov ID
NCT01554930
Collaborator
China Academy of Chinese Medical Sciences (Other), Beijing YouAn Hospital (Other), The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine (Other), Beijing University of Chinese Medicine (Other)
230
3
2
19
76.7
4

Study Details

Study Description

Brief Summary

The study is aimed to evaluate the effectiveness and safety of Xiyanping injection,a traditional Chinese medicine (TCM), in the treatment of severe type of hand, foot, and mouth disease (HFMD).

Condition or Disease Intervention/Treatment Phase
  • Drug: Western therapy (mannitol, methylprednisolone, immunoglobulin, febrifuge)
  • Drug: Xiyanping injection plus western therapy
N/A

Detailed Description

By adopting a multi-center, randomized and controlled clinical trial, this study is aimed to evaluate the effectiveness, safety and economic evaluation of a traditional Chinese medicine, Xiyanping injection,for treatment of HFMD, and to provide scientific evidence for the construction of TCM methods in treating HFMD.

Study Design

Study Type:
Interventional
Actual Enrollment :
230 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Clinical Trial to Evaluate the Effectiveness and Safety of Chinese Medicine in the Treatment of Severe Type of Hand, Foot, and Mouth Disease
Study Start Date :
May 1, 2010
Actual Primary Completion Date :
Nov 1, 2010
Actual Study Completion Date :
Dec 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Western therapy

Drug: Western therapy (mannitol, methylprednisolone, immunoglobulin, febrifuge)
Mannitol:0.5-1.0g/kg,q4h to q8h ivgtt; Methylprednisolone:1mg-2mg/kg·d,qd iv; Immunoglobulin:1g/kg; Others:febrifuge,sedative,etc.

Experimental: Xiyanping injection plus western therapy

Drug: Xiyanping injection plus western therapy
Xiyanping injection:5-10mg/kg/d (0.2-0.4ml/kg/d),qd ivgtt; Mannitol:0.5-1.0g/kg,q4h to q8h ivgtt; Methylprednisolone:1mg-2mg/kg·d,qd iv; Immunoglobulin:1g/kg; Others:febrifuge,sedative,etc.

Outcome Measures

Primary Outcome Measures

  1. complication rate [15 days]

    Refering to the ratio of patient having complications such as pulmonary edema, myocarditis,damage of central nervous system,shock, respiratory failure, multiple organ failur etc.

Secondary Outcome Measures

  1. time of body temperature going back to normal [15 days]

    Refering to the time of the armpit temperature of lower than 37.0 degrees Celsius, lasting for at least 24 hours, after the medicine is taken.

  2. time of symptom disappearance [15 days]

    Referring to the length of time when clinical symptoms and signs totally disappear after the medicine is used.

  3. safety outcome [15 days]

    Calculated by adverse event

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Year to 13 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinical diagnosis of severe hand-foot-mouth disease patients according to Hand-Foot-Mouth Disease Treatment Guidelines 2010 issued by China's Ministry of Health; More than 1/3 patients should be diagnosed by etiological examination.

  • Less than 24 hours of occurrence of fever and/or occurrence of tetter or herpes.

  • Age of 1-13 years.

  • Patients or their guardians agree to participate in this study and signed the informed consent form.

Exclusion Criteria:
  • Complicated with other diseases such as neurogenic pulmonary edema, cardiopulmonary failure.

  • Complicated with other serious primary diseases in organ such as congenital heart disease, chronic hepatitis, nephritis and blood diseases, etc.

  • With history of allergies on traditional Chinese medicine.

  • Patients who using glucocorticoids for based diseases.

  • Patients who having history of hemolysis.

  • Patients or their guardians suffering from Psychiatric diseases.

  • Attending other clinical studies on HFMD after diagnosed.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Liuzhou People's Hospital Liuzhou Guangxi China
2 Handan Maternal and Child Health Care Hospital Handan Hebei China
3 Jiangxi Children's Hospital Nanchang Jiangxi China

Sponsors and Collaborators

  • Jiangxi Qingfeng Pharmaceutical Co. Ltd.
  • China Academy of Chinese Medical Sciences
  • Beijing YouAn Hospital
  • The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine
  • Beijing University of Chinese Medicine

Investigators

  • Study Chair: Li Xiu hui, PhD, Beijing You-An Hospital
  • Study Chair: Zhang Guo liang, PhD, The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine
  • Principal Investigator: Shi Qin sheng, PhD, Handan Maternal and Child Health Care Hospital
  • Principal Investigator: Zhu Qin xiong, PhD, Jiangxi Children's Hospital
  • Principal Investigator: Yang tong, PhD, LiuZhou People's Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jiangxi Qingfeng Pharmaceutical Co. Ltd.
ClinicalTrials.gov Identifier:
NCT01554930
Other Study ID Numbers:
  • 200907001-3
First Posted:
Mar 15, 2012
Last Update Posted:
Mar 15, 2012
Last Verified:
Mar 1, 2012

Study Results

No Results Posted as of Mar 15, 2012