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NCT01866982 · ClinicalTrials.gov registry record · NA

The PREMOD Trial: A Randomized Controlled Trial of Umbilical Cord Milking vs. Delayed Cord Clamping in Premature Infants

A NA study of Intraventricular Hemorrhage, sponsored by Sharp HealthCare.

Completed
Registry status
NA
Development phase
197
Enrollment target
3
Study locations

NCT01866982 is a NA study of Intraventricular Hemorrhage that has completed, run by Sharp HealthCare. The registered enrollment target is 197 participants, below the 1,196-participant average among 11 other Intraventricular Hemorrhage trials with a reported enrollment target (84% lower). The trial reports 3 study locations across 1 state.

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The verdict

NCT01866982, a NA study of Intraventricular Hemorrhage, has completed, sponsored by Sharp HealthCare.

COMPLETED
Registry status
NA
Development phase
197 participants
Enrollment target
3
Study locations

Study Summary

Premature babies can be very sick and have bleeding in the brain. Giving babies more blood before cutting the umbilical cord by delayed cord clamping or umbilical cord milking has been shown to reduce the risk of bleeding in the brain. This may be related to improving perfusion to the brain. However, some studies suggest that delayed cord clamping may not increase hemoglobin or blood volume in babies delivered by cesarean section. Milking the umbilical cord may give more blood in babies delivered by Cesarean Section may improve perfusion and reduce bleeding in the brain.

Interventions

  • PROCEDURE Umbilical Cord Milking
  • PROCEDURE Delayed Cord Clamping

Study Locations (3)

California

  • Loma Linda Medical Center - Loma Linda
  • Sharp Mary Birch - San Diego
  • University of California, San Diego - San Diego

Trial Details

FieldValue
Enrollment Target 197 participants
Start Date 2013-07-02
Est. Completion 2018-01-10
Phase NA

Sponsor

Sharp HealthCare

32 total trials

What the Registry Record Tells You About NCT01866982

The ClinicalTrials.gov registry entry for NCT01866982 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 197 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,196-participant average among 11 other Intraventricular Hemorrhage trials with a reported enrollment target (84% lower). The listed sponsor is Sharp HealthCare, which has 32 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Intraventricular Hemorrhage appearing as the primary indexed condition, and to 2 interventions - of which Umbilical Cord Milking is the first listed.

NCT01866982 reports 3 study locations spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT01866982 about?

NCT01866982 is a clinical study titled "The PREMOD Trial: A Randomized Controlled Trial of Umbilical Cord Milking vs. Delayed Cord Clamping in Premature Infants". Premature babies can be very sick and have bleeding in the brain. Giving babies more blood before cutting the umbilical cord by delayed cord clamping or umbilical cord milking has been shown to reduce the risk of bleeding in the brain. This may be related to improving perfusion to the brain. However...

What is the current status of trial NCT01866982?

This trial is currently completed. It is a NA study. The enrollment target is 197 participants. The study started on 2013-07-02. Estimated completion is 2018-01-10.

What conditions does trial NCT01866982 study?

This clinical trial studies the following conditions: Intraventricular Hemorrhage.

What interventions are being tested in trial NCT01866982?

The interventions under investigation include: Umbilical Cord Milking (PROCEDURE), Delayed Cord Clamping (PROCEDURE).

Who is sponsoring clinical trial NCT01866982?

This trial is sponsored by Sharp HealthCare, which has 32 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01866982 being conducted?

This trial has 3 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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