Clinical Trials Directory

Trials / Terminated

TerminatedNCT00266942

Intra-Atrial vs. Extra-Cardiac Technique During Fontan Operation

The Determination of Differences Between Intr-Atrial vs. Extra-Cardiac Technique During the Fontan Operation: A Retrospective Review

Status
Terminated
Phase
Study type
Observational
Enrollment
400 (planned)
Sponsor
Children's Healthcare of Atlanta · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Our aim is a retrospective chart review seeking to determine any differences in the main clinical and outcome variables as well as general outcome data such as functional recovery, readmission rates, somatic growth and mortality. An n size of 150 to 200 for each of the 2 groups will give us excellent power to detect potential differences.

Detailed description

The Fontan procedure is indicated as final-stage treatment for pediatric cardiac patients with single ventricle physiology. This procedure, whose aim is to provide for total cavopulmonary disconnect and perfusion of the pulmonary arteries via systemic veins, is performed via two differing techniques: intra-atrial, so-called lateral tunnel technique, employing PTFE graft material and internal atrial baffle, versus the extracardiac technique, using larger PTFE tubing and externally constructed baffle. There is persistent debate regarding the optimal technique to use, centered around the following main issues: 1) need for use of cardiopulmonary bypass and attendant consequences, 2) rates of thrombosis and embolism, 3) incidence of postoperative protein-losing enteropathy (PLE), 4) incidence of arrhythmias, and 5) baffle patency rates. A handful of small- to medium-sized studies has addressed the above issues, but, importantly, has not used patient data from the same institution. Here at CHOA, there are an estimated 200+ lateral tunnel, and have been up to 125 to 150 extracardiac Fontan procedures, performed in the last 15 years (1.1.1980-3.31.2005). Data from these cases would be potentially very helpful in answering all of these questions.

Conditions

Timeline

Start date
1990-01-01
Completion
2007-01-01
First posted
2005-12-20
Last updated
2007-05-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00266942. Inclusion in this directory is not an endorsement.