Clinical Trials Directory

Trials / Completed

CompletedNCT00569855

Intravenous Phenoxybenzamine Use in Pediatric Patients Undergoing Open-Heart Surgery

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
785 (actual)
Sponsor
University of Arkansas · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Cardiopulmonary bypass is done with a machine that does the work of the heart and lungs during open-heart surgery. This study is to determine if intravenous (i.v.) phenoxybenzamine is safe. This drug lowers the blood pressure, making it easier for the cardiopulmonary bypass machine to deliver blood and oxygen to all of the organs and tissues.

Conditions

Interventions

TypeNameDescription
DRUGPhenoxybenzamine0.125 to 1 mg/kg given i.v. over 15 to 45 minutes in preparation for cardiopulmonary bypass; may be continued at 0.125 mg/kg/day in ICU

Timeline

Start date
2001-02-01
Primary completion
2010-08-01
Completion
2010-08-01
First posted
2007-12-10
Last updated
2011-03-01
Results posted
2011-03-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00569855. Inclusion in this directory is not an endorsement.