Status:
UNKNOWN
Noninvasive Continuous Measurement of SpHb After Spontaneous Vaginal Delivery
Lead Sponsor:
Città di Roma Hospital
Conditions:
Delivery Uterine
Eligibility:
FEMALE
18-40 years
Phase:
NA
Brief Summary
Aim of this study is to determine the physiological reference individual values (RI) of maternal continuous SpHb immediately after delivery in the post-partum period (continuous monitoring up to 2 hou...
Detailed Description
Background and Significance: Pregnancy and childbirth involve health risks, even for women without any pre-existing health problems. Postpartum hemorrhage is one of most common complications for deli...
Eligibility Criteria
Inclusion
- Healthy parturients in labor
Exclusion
- Parturient with coagulation defects, or with anticoagulant therapy
Key Trial Info
Start Date :
December 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 1 2012
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT01505192
Start Date
December 1 2011
End Date
May 1 2012
Last Update
January 6 2012
Active Locations (1)
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1
Città di Roma Hospital
Roma, Italy