Clinical Trials Directory

Trials / Completed

CompletedNCT00006330

Pharmacokinetic and Pharmacodynamic Interaction Study of Digoxin and Hawthorn

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
Sponsor
National Center for Research Resources (NCRR) · NIH
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

Hawthorn (Crataegus oxyacantha) is a natural product that is popular in European and American herbal medicine practice. Some of its cardiac uses include the treatment of high and low blood pressure, rapid heart beat, chest pain, and blocked arteries. In many cases, it is used as an adjuvant agent with other cardiac drugs such as digoxin, amiodarone, and warfarin. To date, little information is known about the effect of hawthorn when taken with other drugs and if toxicities occur when hawthorn is used with other drugs. The purpose of this study is to examine the interaction between digoxin and hawthorn in eight healthy subjects. Subjects will be recruited by advertisement. The design of the study will include a 10-day and a three-week treatment phase of digoxin 0.125 mg - 0.25 mg/day and hawthorn (Crataegus special extract WS1442, Schwabe Co.) 450 mg twice daily or placebo, with a randomized crossover. There will be a three-week washout period in between treatment phases. On day 10 (phase I) and day 21 (phase II), subjects will have 12 blood samples drawn for pharmacokinetic analysis. The plasma samples will be measured for digoxin concentration. Additionally, the subjects will be assessed for any clinical toxicities or adverse events. The significance of this study is to provide the clinician with information regarding the safe use of digoxin in combination with the herbal supplement, hawthorn.

Conditions

Interventions

TypeNameDescription
DRUGDigoxin
DRUGHawthorn

Timeline

First posted
2000-10-05
Last updated
2005-06-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00006330. Inclusion in this directory is not an endorsement.