NCT00329212

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.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 23, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

May 24, 2006

Completed
Last Updated

November 15, 2006

Status Verified

November 1, 2006

First QC Date

May 23, 2006

Last Update Submit

November 14, 2006

Conditions

Healthy

Keywords

PharmacokineticsBioavailabilityTherapeutic Equivalency

Interventions

San Huang Xie Jin TangDRUG

Eligibility Criteria

Age20 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Committee on Chinese Medicine and Pharmacy, Department of Health

Taipei, Taiwan, China

Location

Study Officials

  • Y C Hou, Professor

    School of Chinese Medicine, China Medical University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
DEFINED POPULATION
Time Perspective
OTHER
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

May 23, 2006

First Posted

May 24, 2006

Last Updated

November 15, 2006

Record last verified: 2006-11

Locations

CN(1)