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 |
---|---|---|
|
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