Status:

WITHDRAWN

Parenteral Phenoxybenzamine During Congenital Heart Disease Surgery

Lead Sponsor:

Vanderbilt University

Conditions:

Congenital Heart Disease

Eligibility:

All Genders

Up to 6 years

Phase:

PHASE2

Brief Summary

Phenoxybenzamine, an irreversible alpha-adrenergic blocker, may prove beneficial to infants and children with congenital heart disease undergoing open cardiac repair, due to a theoretic benefits of a ...

Detailed Description

II. Background 1. Description of the Problem One of the effects of cardiac operations involving cardiopulmonary bypass is reversible myocardial dysfunction lasting a number of days postoperatively. T...

Eligibility Criteria

Inclusion

  • Patient selection will be determined by an assessment of the risk of systemic ventricular dysfunction following open cardiac repair in a population of infants undergoing stage I palliation (Norwood procedure) for the diagnosis of either hypoplastic left heart syndrome or similar left-sided obstructive lesions in the setting of single-ventricle physiology. Eligible neonates and infants include those aged 0 days to 6 months. These patients will be evaluated on an individual basis and the decision to give phenoxybenzamine would be determined by the attending surgeon, anesthesiologist, and cardiologist.

Exclusion

    Key Trial Info

    Start Date :

    October 1 2008

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    August 1 2010

    Estimated Enrollment :

    Patients enrolled

    Trial Details

    Trial ID

    NCT00770705

    Start Date

    October 1 2008

    End Date

    August 1 2010

    Last Update

    May 1 2017

    Active Locations (1)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 1 (1 locations)

    1

    Vanderbilt Children's Hospital

    Nashville, Tennessee, United States, 37232

    Parenteral Phenoxybenzamine During Congenital Heart Disease Surgery | DecenTrialz