Multisite Feeding Study: Home Surveillance and Feeding Strategies in Infants With Complex Single Ventricle

Home Surveillance and Feeding Strategies in Infants With Complex Single Ventricle

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00257517

Enrollment

Registered

2005-11-23

Start date

2005-10-31

Completion date

2010-06-30

Last updated

2014-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital Disorders

Keywords

Congenital heart disease, Single ventricle, Infant feeding

Brief summary

This study will assess 75-100 patients for feeding issues following surgery for single ventricle.

Detailed description

We wish to consent 75-100 subjects at Children's Healthcare of Atlanta. If subjects take part in this study, the following will happen: 1. Prior to discharge, the parent/guardian will be given a home feeding log and 2. Parents will bring the feeding log to regularly scheduled clinic visits. Clinic staff will also weigh the child and measure head circumference at each clinic visit. 3. The investigators will look at the child's medical record to obtain other information including diagnosis, surgery, oxygen saturation levels and medications. 4. The parent/guardian will be asked to fill out a questionnaire about their stress and uncertainty caring for their baby after heart surgery. They will be asked to fill out the same questionnaire 3 times: * First time will be before they leave the hospital after the baby's surgery, while still a patient on the Cardiac Step Down Unit (CSU). * Second time will be at the Sibley Heart Center Cardiology clinic after they have been home for approximately 4 weeks. * Third time will be at the Sibley Heart Center Cardiology clinic after they have been home for approximately 12 weeks or at the time of the routine cardiac cath prior to their second stage surgery. It should take about 15 minutes to fill out the questionnaire. The questionnaire is the only research procedure. The data from the feeding log and clinic visits will be submitted to Cincinnati Children's, the primary site for this study.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

No minimum to 30 Days

Healthy volunteers

Inclusion criteria

* Single ventricle patients who have received the Norwood Stage I operation.

Exclusion criteria

* Infants with chromosomal anomalies or other non-cardiac conditions (cleft palate, necrotizing enterocolitis \[NEC\] or other gastrointestinal \[GI\] anomalies) * Prematurity less than 37 weeks * Infants greater than 30 days of age at Stage I palliation * Parents who cannot read or understand questionnaires administered as a part of the study.

Design outcomes

Primary

Measure	Time frame
weight gain	5 months

Countries

United States

Outcome results