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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00071682
Other study ID # K08AT001338-01
Secondary ID K08AT001338-01
Status Withdrawn
Phase N/A
First received October 29, 2003
Last updated May 13, 2013
Start date October 2007
Est. completion date December 2007

Study information

Verified date May 2013
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine if the use of herbal products interferes with normal anticoagulation, leading to either excessive thinning of the blood and bleeding problems or inadequate thinning of the blood and clotting problems. Many patients who are on long term anticoagulation, or blood thinning, for a variety of medical problems, also take herbal products. It is not yet known whether use of herbal products interferes with this anticoagulation, and puts patients at risk for bleeding or clotting. This study will carefully monitor patients who are taking herbs and anticoagulants to determine if their laboratory tests show signs of being affected by the herbs. The study will ask all patients about their herbal product use, so all reported herbs will be included and monitored.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2007
Est. primary completion date December 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

- Taking longer-term (>6 months) anticoagulation

- Enrolled in one of Kaiser Permanente Northern California anticoagulation clinics

Study Design

Time Perspective: Prospective


Locations

Country Name City State
United States San Francisco VA Medical Center San Francisco California

Sponsors (2)

Lead Sponsor Collaborator
University of California, San Francisco National Center for Complementary and Integrative Health (NCCIH)

Country where clinical trial is conducted

United States,