Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Recruiting Not applicable Interventional

Cord Clamping Among Neonates With Congenital Heart Disease

ClinicalTrials.gov ID: NCT06153459

Public ClinicalTrials.gov record NCT06153459. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 1:56 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

CORD-CHD: Clamp OR Delay Among Neonates With Congenital Heart Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this clinical trial is to compare 2 different timepoints for clamping the umbilical cord at birth for term-born infants with a prenatal diagnosis of congenital heart disease (CHD). The main questions it aims to answer are: * Does Delayed Cord Clamping at 120 seconds (DCC-120) or Delayed Cord Clamping at 30 seconds (DCC-30) after birth lead to better health outcomes? * Does DCC-120 seconds or DCC-30 seconds after birth lead to better neuromotor outcomes at 22-26 months of infant age (postnatal)? Participants will be asked to do the following: * Participate in either DCC-120 or DCC-30 at birth (randomized assignment). * Complete General Movements Assessment (GMA) at 3-4 months of infant age (postnatal), complete questionnaires / surveys at this time. * Complete questionnaires / surveys at 9-12 months of infant age (postnatal). * Complete Hammersmith Infant Neurological Examination (HINE), Developmental Assessment of Young Children 2 Edition (DAYC-2), and questionnaires / surveys at 22-26 months of infant age (postnatal). * Permit data collection from electronic medical records for both the mother and infant study participants. Investigators will compare DCC-120 vs. DCC-30 to see which approach is more beneficial to both the mother and baby with CHD.

Study identification

NCT ID
NCT06153459
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Carl Backes, MD
Other
Enrollment
500 participants

Conditions and interventions

Eligibility (public fields only)

Age range
37 Weeks to 42 Weeks
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 18, 2023
Primary completion
Sep 30, 2028
Completion
Nov 30, 2030
Last update posted
Aug 11, 2026

2023 – 2030

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Children's of Alabama Birmingham Alabama 35233 Recruiting
Cedars-Sinai Medical Center Los Angeles California 90048 Recruiting
Children's Hospital of Orange County Orange California 92868 Not yet recruiting
Lucile Packard Children's Hospital Stanford Palo Alto California 94304 Not yet recruiting
Sharp Mary Birch Hospital for Woman and Newborns San Diego California 92123 Recruiting
UF Health Shands Children's Hospital Gainesville Florida 32608 Recruiting
Johns Hopkins Children's Center Baltimore Maryland 21287 Recruiting
Children's of Mississippi Jackson Mississippi 39216 Recruiting
The Children's Mercy Hospital Kansas City Missouri 64108 Recruiting
SSM Health Cardinal Glennon Children's Hospital St Louis Missouri 63104 Recruiting
Duke Children's Hospital & Health Center Durham North Carolina 27705 Recruiting
Nationwide Children's Hospital Columbus Ohio 43205 Recruiting
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104 Recruiting
Medical University of South Carolina Columbia South Carolina 29209 Recruiting
Monroe Carell Jr. Children's Hospital at Vanderbilt Nashville Tennessee 37232 Recruiting
Texas Children's Hospital Houston Texas 77030 Recruiting
University of Texas Health Science Center at San Antonio San Antonio Texas 78229 Recruiting
Primary Children's Hospital Salt Lake City Utah 84113 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06153459, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 11, 2026 · Synced Sep 2, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06153459 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →