Status:
WITHDRAWN
Timing of Cord Clamping and Neonatal Hemoglobin
Lead Sponsor:
Oklahoma State University Center for Health Sciences
Conditions:
Anemia
Eligibility:
FEMALE
18-34 years
Phase:
NA
Brief Summary
The purpose of this study is to determine whether the timing of the clamping of the umbilical cord after delivery has an impact on neonatal hemoglobin and hematocrit, tests that determine the number o...
Detailed Description
The purpose of this study is to determine whether the timing of the clamping of the umbilical cord after delivery has an impact on neonatal hemoglobin and hematocrit, tests that determine the number o...
Eligibility Criteria
Inclusion
- Healthy women and their newborn infants delivered at Tulsa Regional Medical Center,
- between the ages of 18 and 34,
- full term (37 to 41 weeks),
- singleton pregnancy at the time of delivery
Exclusion
- Delivery complicated by non-reassuring fetal heart tones,
- preeclampsia,
- eclampsia,
- chronic hypertension,
- meconium-stained amniotic fluid,
- fetal anomalies or
- any other condition which could require immediate newborn evaluation by nursery personnel at the time of delivery. Infants requiring operative delivery by forceps or vacuum also will be excluded.
Key Trial Info
Start Date :
September 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2009
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00371228
Start Date
September 1 2006
End Date
June 1 2009
Last Update
October 5 2020
Active Locations (1)
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1
OSU Houston Center
Tulsa, Oklahoma, United States, 74127