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Clinical Trial Summary

The purpose of this initiative is to improve care and outcomes for infants with HLHS by expanding the NPC-QIC national registry to gather clinical care process, outcome, and developmental data on infants with HLHS between diagnosis and 12 months of age, by improving the use of standards into everyday practice across pediatric cardiology centers, and by engaging parents as partners in the process.


Clinical Trial Description

The purpose of this initiative is to improve care and outcomes for infants with HLHS by: 1) expanding the established NPC-QIC national registry to gather clinical care process, outcome, and developmental data on infants with HLHS between diagnosis and 12 months of age, 2) improving implementation of consensus standards, tested by teams, into everyday practice across pediatric cardiology centers, and 3) engaging parents as partners in improving care and outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02852031
Study type Observational [Patient Registry]
Source Children's Hospital Medical Center, Cincinnati
Contact Mark Timbers
Email mark.timbers@cchmc.org
Status Recruiting
Phase
Start date May 2016
Completion date May 2028

See also
  Status Clinical Trial Phase
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