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NCT00329212 Clinical Trial

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

Healthy Clinical Trial

Official title:
Bioequivalence of Bioactive Markers Between Concentrated Herbal Formula and Traditional Herbal Decoctions in Humans

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00329212
Other study ID # CCMP95-RD-010
Secondary ID
Status Completed
Phase N/A
First received May 23, 2006
Last updated November 14, 2006

Study information
Verified date November 2006
Source Committee on Chinese Medicine and Pharmacy
Contact n/a
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- The volunteers about 6~8 persons should be aged from 20 to 35 years old with a body weight between 50~80 kg, no marriage and have a healthy body condition.

Study Design

Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Intervention

Drug:
• San Huang Xie Jin Tang

Locations
Country Name City State
China Committee on Chinese Medicine and Pharmacy, Department of Health Taipei Taiwan

Sponsors (1)
Lead Sponsor Collaborator
Committee on Chinese Medicine and Pharmacy

Country where clinical trial is conducted

China, 

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