NCT00251602View on ClinicalTrials.gov

Analysis of Atropine and Propranolol Induced Changes

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

March 31, 2003

Primary Completion Date

August 31, 2012

Study Completion Date

August 31, 2012

Conditions
Healthy
Interventions
DRUG

Atropine

One-time 10 mcg/kg infusion over 30 minutes, followed by a 10 mcg/kg bolus

DRUG

Propranolol

One-time 0.8mg/kg/hr infusion (maximum dose not to exceed 20mg) over 20 minutes, followed by either atropine or normal saline

DRUG

Normal Saline

One-time 0.25 ml/min infusion over 30 minutes

Trial Locations (1)

21225

National Institute on Aging, Harbor Hospital, Baltimore

All Listed Sponsors
lead

National Institute on Aging (NIA)

NIH

NCT00251602 - Analysis of Atropine and Propranolol Induced Changes | Biotech Hunter | Biotech Hunter