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NCT03741803 · ClinicalTrials.gov registry record · NA

Relationship Between Delayed Cord Clamping at Birth and Neonatal Bilirubin Levels in Parturients With a Prior Child Requiring Therapy for Neonatal Jaundice

A NA study, sponsored by The University of Texas Health Science Center, Houston.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT03741803 is a NA study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 20 participants.

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The verdict

NCT03741803, a NA study, has completed, sponsored by The University of Texas Health Science Center, Houston.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

The purpose of the study is to determine if neonates (who already have an increased risk of hyperbilirubinemia due to mother's history of having previous neonate who received phototherapy for hyperbilirubinemia) have higher bilirubin levels 24 hours after birth with delayed cord clamping.

Interventions

  • PROCEDURE Delayed cord clamping
  • PROCEDURE Early cord clamping

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2018-11-09
Est. Completion 2019-05-27
Phase NA

What the Registry Record Tells You About NCT03741803

The ClinicalTrials.gov registry entry for NCT03741803 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Delayed cord clamping is the first listed.

NCT03741803 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03741803 about?

NCT03741803 is a clinical study titled "Relationship Between Delayed Cord Clamping at Birth and Neonatal Bilirubin Levels in Parturients With a Prior Child Requiring Therapy for Neonatal Jaundice". The purpose of the study is to determine if neonates (who already have an increased risk of hyperbilirubinemia due to mother's history of having previous neonate who received phototherapy for hyperbilirubinemia) have higher bilirubin levels 24 hours after birth with delayed cord clamping.

What is the current status of trial NCT03741803?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2018-11-09. Estimated completion is 2019-05-27.

What interventions are being tested in trial NCT03741803?

The interventions under investigation include: Delayed cord clamping (PROCEDURE), Early cord clamping (PROCEDURE).

Who is sponsoring clinical trial NCT03741803?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.