Analysis of Atropine and Propranolol Induced Changes

Completed · Phase 1

Conditions studied: Healthy

In brief

The purpose of this study is to learn the effects of genetic make up on response to the drugs atropine and propranolol, to examine how changes in heart rate and blood pressure can be measured, and to test a new statistical analysis method.

Key facts

Study ID

NCT00251602

Run by

National Institute on Aging (NIA)

People needed

24

Starts

2003-03-01

Expected to finish

2012-08-01

Last updated by the study team

2012-08-06

Who can join

Age: 21 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy male and female volunteers
• Ages 21-40
• Body Mass Index >18.0 and <27.0

You may not qualify if…

• History of any chronic illnesses including cardiac diseases and bleeding problems
• Drug use of any kind
• Participation in any clinical trial within the last month
• Tobacco use and/or alcohol abuse
• Use of dietary supplements and unwillingness to refrain

Where it is running

• National Institute on Aging, Harbor Hospital — Baltimore, Maryland, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.