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NCT03150641

Delayed Cord Clamping at Term Cesarean

Completed NA Last updated 22 May 2019
What this trial tests

NA trial testing Umbilical cord clamping in Maternal Blood Loss in 113 participants. Completed in 31 March 2018.

Timeline
18 September 2017
Primary endpoint
30 March 2018
31 March 2018

Quick facts

Lead sponsorColumbia University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment113
Start date18 September 2017
Primary completion30 March 2018
Estimated completion31 March 2018
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Columbia University

Who can join

Adults 18 to 60, female only, with Maternal Blood Loss or Cesarean Delivery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this research study is to find out how delaying cutting the umbilical cord until one minute after delivery of the baby during a cesarean impacts the amount of blood the mother loses during surgery. The study will also examine the benefits to the newborn from delayed cord clamping during cesarean.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Effect of Delayed vs Immediate Umbilical Cord Clamping on Maternal Blood Loss in Term Cesarean Delivery: A Randomized Clinical Trial.
    Purisch SE, Ananth CV, Arditi B, Mauney L, et al · · 2019 · cited 48× · PMID 31742629 · DOI 10.1001/jama.2019.15995

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03150641.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing