Milking the Umbilical Cord at Term Cesarean Birth
Completed · Early Phase 1
Conditions studied: Anemia
In brief
The purpose of this pilot study is to determine if umbilical cord milking at the time of scheduled cesarean section effects the hemoglobin and hematocrit levels of full-term infants as determined by hemoglobin and hematocrit levels at 36-48 hours of life. This study will help to establish the feasibility of umbilical cord milking as an alternative to delayed clamping at the time of planned cesarean section.
Key facts
- Study ID
- NCT01630993
- Run by
- University of Rhode Island
- People needed
- 24
- Starts
- 2008-05-01
- Expected to finish
- 2009-12-01
- Last updated by the study team
- 2015-10-05
Who can join
Age: 18 and older, up to 44. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Women at full term gestation (37-41 weeks) with:
- Uncomplicated, singleton pregnancy
- English speaking
- Planning an elective Cesarean Section
- Not in labor
You may not qualify if…
- Major medical or obstetrical complications
- Women who smoke
- Intrauterine growth restriction
- Serious congenital anomalies
Where it is running
- Women & Infants Hospital — Providence, Rhode Island, United States
Full record on ClinicalTrials.gov
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