Status:
WITHDRAWN
Comparison of Two Fetal Lung Maturity Tests
Lead Sponsor:
Oklahoma State University Center for Health Sciences
Conditions:
Respiratory Distress Syndrome
Eligibility:
FEMALE
Brief Summary
The investigators wish to compare the difference in both cost and time to result for determining fetal lung maturity for the Lamellar Body Count method and the Fetal Lung Maturity II. Our hypothesis i...
Detailed Description
Rationale/Background: This pilot study is a prospective cohort analysis of two methods currently available at our institution for the determination of fetal lung maturity (FLM) using amniotic fluid. T...
Eligibility Criteria
Inclusion
- Term intrauterine gestations beyond 37 completed weeks with dating calculated by their sure last menstrual period (LMP) using Negel's rule or utilizing a first trimester crown rump length ultrasound.
- Women with a previous C/S scheduled for repeat C/S.
- Women who are undergoing a scheduled C-Section for malpresentation
Exclusion
- Presence of gross blood in amniotic sample
- Hematocrit count greater than 1% on ADVIA 2120
- Presence of meconium in sample
- Patients with oligohydramnios defined as an amniotic fluid index of less than 5 cm or polyhydramnios defined as an amniotic fluid index of more than 24 cm.
Key Trial Info
Start Date :
January 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
May 1 2010
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00613977
Start Date
January 1 2008
End Date
May 1 2010
Last Update
October 5 2020
Active Locations (1)
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1
Oklahoma State University Medical Center
Tulsa, Oklahoma, United States, 74103