Changes in Cardiac Output During Delayed Umbilical Cord Clamping
NCT ID: NCT02195037
Last Updated: 2015-05-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
20 participants
OBSERVATIONAL
2014-07-31
2014-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Delivered by vaginal birth
* Estimated gestational age of 37+0to 41+6 weeks corrected gestational age
Exclusion Criteria
* Known fetal anomalies (including cardiac defects).
* Instrumentation during delivery (forceps or vacuum)
* Non-reducible nuchal cord during delivery.
* Any maternal or neonatal indication requiring immediate cord clamping.
1 Minute
ALL
No
Sponsors
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Sharp HealthCare
OTHER
Responsible Party
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Anup Katheria, M.D.
Director of Neonatal Research
Principal Investigators
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Anup Katheria, MD
Role: PRINCIPAL_INVESTIGATOR
Sharp HealthCare
Locations
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Sharp Mary Birch Hospital for Women and Newborns
San Diego, California, United States
Countries
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References
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Katheria AC, Wozniak M, Harari D, Arnell K, Petruzzelli D, Finer NN. Measuring cardiac changes using electrical impedance during delayed cord clamping: a feasibility trial. Matern Health Neonatol Perinatol. 2015 May 22;1:15. doi: 10.1186/s40748-015-0016-3. eCollection 2015.
Other Identifiers
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CO-DCC
Identifier Type: -
Identifier Source: org_study_id
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