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Comparative Outcomes Related to Delivery-room Cord Milking In Low-resourced Kountries- PreTerm

Study acronym: CORDMILK-PT
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion date: Jun 30, 2026 to Nov 30, 2026
    • Study completion date: Dec 30, 2026 to Mar 30, 2027
    v6
  2. Study sites: 8 to 9
    • Collaborators: 10 to 11
    v5
  3. Trial status: Not Yet Recruiting to Recruiting
    • Site details revised at 8 of 8 sites
    v4
  4. Start date: Jun 1, 2024 to Jul 1, 2024
    • Primary completion date: May 28, 2026 to Jun 30, 2026
    v3
  5. Start date: Mar 1, 2024 to Jun 1, 2024
    • Primary completion date: Feb 28, 2026 to May 28, 2026
    • Study completion date: Sep 30, 2026 to Dec 30, 2026
    v2
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this multicenter, cluster-randomized, crossover trial is to determine if umbilical cord milking compared to early cord clamping will reduce in-hospital mortality in non-vigorous preterm infants born between 30 weeks and 34 weeks of gestation.
Trial Details
NCT Number NCT06240715
Lead Sponsor Nemours Children's Clinic
Collaborators: Thrasher Research Fund, Thomas Jefferson University, Sharp HealthCare, Jawaharlal Nehru Medical College, Daga Memorial Maternity and Children's Hospital, Nagpur, India, Mahatma Gandhi Institute of Medical Sciences, Indira Gandhi Government Medical College & Hospital, Nagpur, India, Pimpri Chinchwad Municipal Corporation's Post-Graduate Institute, Yashwantrao Chavan Memorial Hospital, Pune, India, Government Medical College, Nagpur, Government Medical College, Chandrapur, India, Osmania Medical College, Niloufer Hospital, Hyderabad, India
Conditions
(from sponsor)		 Preterm, Infant Death
Related terms Fetofetal Transfusion, Infant Death, Premature Birth
Enrollment 800 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov