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Completed Not applicable Interventional

Premature Infants Receiving Milking or Delayed Cord Clamping: PREMOD2

ClinicalTrials.gov ID: NCT03019367

Public ClinicalTrials.gov record NCT03019367. 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 Oct 22, 2026, 4:59 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

Premature Infants Receiving Milking or Delayed Cord Clamping: Randomized Controlled Multicenter Non-inferiority Trial

Brief summary

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

This study is being done to find out whether umbilical cord milking (UCM) is at least as good as or better than delayed cord clamping (DCC) to reduce bleeding in the brain or prevent death in premature newborns. The investigators will study short and long term outcomes of infants delivered before 32 weeks gestation that receive either UCM or DCC. \* The trial was stopped by the DSMB for safety in the small strata. They subsequently allowed for continuation of the trial in infants 29-32+6 wk GA.

Study identification

NCT ID
NCT03019367
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Sharp HealthCare
Other
Enrollment
1,201 participants

Conditions and interventions

Eligibility (public fields only)

Age range
23 Weeks to 33 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
Jun 6, 2017 (Actual)
Primary completion
Sep 16, 2022 (Actual)
Completion
Sep 16, 2022 (Actual)
Last update posted
Nov 23, 2022

2017 – 2022

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294-0004 —
Loma Linda Medical Center Loma Linda California 92350 —
LAC+USC Medical Center Los Angeles California 90033 —
PIH Health Good Samaritan Hospital Los Angeles California 90033 —
University of California, Irvine Medical Center Orange California 92868 —
Sharp Grossmont Hospital San Diego California 91942 —
Sharp Mary Birch Hospital for Women and Newborns San Diego California 92123 —
Christiana Care Newark Delaware 19718 —
John H. Stroger, Jr. Hospital of Cook County Chicago Illinois 60612 —
University of Mississippi Medical Center Jackson Mississippi 39216 —
St. Louis University St Louis Missouri 63104 —
Cincinnati Children's Hospital Cincinnati Ohio 45229 —
Providence St. Vincent Medical Center Portland Oregon 97225-6603 —
Magee-Womens Hospital Pittsburgh Pennsylvania 15213 —
University of Utah Salt Lake City Utah 84112 —

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 NCT03019367, 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 Nov 23, 2022 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03019367 live on ClinicalTrials.gov.

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