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NCT01749059 · ClinicalTrials.gov registry record

The Impact of Implementing a Universal Newborn Screening for Critical Congenital Heart Disease

A clinical trial of Congenital Heart Disease, sponsored by Pediatrix.

Completed
Registry status
6,147
Enrollment target
1
Study location

NCT01749059: Completed study of Congenital Heart Disease, sponsored by Pediatrix.

NCT01749059 is a study of Congenital Heart Disease that has completed, run by Pediatrix. The registered enrollment target is 6,147 participants, above the 376-participant average among 63 other Congenital Heart Disease trials with a reported enrollment target (1535% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01749059, a study of Congenital Heart Disease, has completed, sponsored by Pediatrix.

COMPLETED
Registry status
6,147 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the impact of implementing a universal pulse oximeter screening as a way to detect critical congenital heart disease in otherwise well-appearing newborns.

Primary Outcome

The numbers of subjects who have a positive pulse oximetry screening test and who in follow-up evaluation are found to have CCHD.

Conditions Studied

Study Locations (1)

New Jersey

  • Capital Health Regional Medical Center - Pediatrix Medical Group - Trenton

Trial Details

FieldValue
Enrollment Target 6,147 participants
Start Date 2012-06
Est. Completion 2016-10
Pediatrix

28 total trials

What the finished NCT01749059 record still lists

NCT01749059 is an observational study that tracks outcomes without assigning an intervention. Its 6,147 participants enrollment target places it among the larger protocols in the corpus, above the 376-participant average among 63 other Congenital Heart Disease trials with a reported enrollment target (1535% higher).

The record links to 1 condition, with Congenital Heart Disease appearing as the primary indexed condition, and to 0 interventions.

NCT01749059 reports a single indexed study location in New Jersey.

Frequently Asked Questions

What is clinical trial NCT01749059 about?

NCT01749059 is a clinical study titled "The Impact of Implementing a Universal Newborn Screening for Critical Congenital Heart Disease". The purpose of this study is to evaluate the impact of implementing a universal pulse oximeter screening as a way to detect critical congenital heart disease in otherwise well-appearing newborns.

What is the current status of trial NCT01749059?

This trial is currently completed. The enrollment target is 6,147 participants. The study started on 2012-06. Estimated completion is 2016-10.

What conditions does trial NCT01749059 study?

This clinical trial studies the following conditions: Congenital Heart Disease.

Who is sponsoring clinical trial NCT01749059?

This trial is sponsored by Pediatrix, which has 28 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01749059 being conducted?

This trial has 1 study location across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Congenital Heart Disease

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01749059's enrollment target sits among peer trials

6,147 2nd of 63 the highest of 63 other Congenital Heart Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Congenital Heart Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01749059, the US trial registry maintained by the National Library of Medicine. NCT01749059 (large enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.