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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00026013
Other study ID # R21AT000836-01
Secondary ID
Status Completed
Phase N/A
First received November 5, 2001
Last updated August 17, 2006
Start date January 2002
Est. completion date January 2004

Study information

Verified date July 2006
Source National Center for Complementary and Integrative Health (NCCIH)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effects of a common herbal remedy, St. John's Wort, on the effectiveness of birth control pills. St. John's Wort has recently been shown to increase metabolism of some drugs. If it could increase metabolism of oral contraceptives as well, it may increase the risk of contraceptive failure and unintended pregnancy. Study participants will be evaluated for risk of ovulation on oral contraceptives before and during simultaneous therapy with St. John's Wort.


Description:

See Brief Summary


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date January 2004
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Women taking or willing to take low dose oral contraceptives for 5 months

- No contraindications to hormonal contraception

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
hypericum perforatum


Locations

Country Name City State
United States Columbia University Department of Obstetrics & Gynecology New York New York

Sponsors (1)

Lead Sponsor Collaborator
National Center for Complementary and Integrative Health (NCCIH)

Country where clinical trial is conducted

United States, 

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