Managing Cyanosis Following Bidirectional Glenn Operation

Stopped early

Conditions studied: Congenital Disorders

In brief

The purpose of this retrospective study is to review the postoperative medical management of infants who underwent bidirectional Glenn operation from January 1, 2003 to December 31, 2005 who were significantly cyanotic.

Key facts

Study ID

NCT00327886

Run by

Children's Healthcare of Atlanta

People needed

150

Starts

2006-02-01

Expected to finish

2006-02-01

Last updated by the study team

2007-06-13

Who can join

Age: any, up to 1. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Infants
• Bidirectional Glenn operation between 1/1/03-12/31/05
• Significant Cyanosis

You may not qualify if…

• Those who do not meet inclusion criteria.

Where it is running

• Children's Healthcare of Atlanta — Atlanta, Georgia, 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.