The Pharmacokinetics Study of Concentrated Herbal Formula and Traditional Herbal Decoctions in Humans

Sponsor
Committee on Chinese Medicine and Pharmacy (Other)
Overall Status
Completed
CT.gov ID
NCT00329212
Collaborator
(none)
1

Study Details

Study Description

Brief Summary

The purpose of this study is to investigate the pharmacokinetics in humans of San Huang Xie Jin Tang (SHXJT) and evaluate the bioequivalence between herbal concentrate and traditional decoction.

Condition or Disease Intervention/Treatment Phase
  • Drug: San Huang Xie Jin Tang

Study Design

Study Type:
Observational
Observational Model:
Defined Population
Time Perspective:
Other
Official Title:
Bioequivalence of Bioactive Markers Between Concentrated Herbal Formula and Traditional Herbal Decoctions in Humans

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 35 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • The volunteers about 68 persons should be aged from 20 to 35 years old with a body weight between 5080 kg, no marriage and have a healthy body condition.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Committee on Chinese Medicine and Pharmacy, Department of Health Taipei Taiwan China

    Sponsors and Collaborators

    • Committee on Chinese Medicine and Pharmacy

    Investigators

    • Principal Investigator: Y C Hou, Professor, School of Chinese Medicine, China Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00329212
    Other Study ID Numbers:
    • CCMP95-RD-010
    First Posted:
    May 24, 2006
    Last Update Posted:
    Nov 15, 2006
    Last Verified:
    Nov 1, 2006

    Study Results

    No Results Posted as of Nov 15, 2006