A Comparison of Rapid Immunoassays for the Detection of Ruptured Membranes
Completed
- Conditions
- Evidence of Ruptured Membranes in Women Greater Than 15 Weekd
- Registration Number
- NCT02208011
- Lead Sponsor
- Louisiana State University, Baton Rouge
- Brief Summary
Specific objectives include analysis of performance of ROM Plus® in diagnosing ROM, as compared to Amnisure® and the conventional clinical assessment confirmed by a thorough chart review after delivery.
Inclusion Criteria:
* English speaking
* pregnant woman \>15 weeks gestation undergoing an exam for ruptured membranes
Exclusion Criteria:
* Known placental previa
* Active vaginal bleeding
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 140
Inclusion Criteria
- complaint of ruptured membranes
- IUP > 15 weeks gestation
- English speaking, over the age of 18yrs old
Exclusion Criteria
- active bleeding
- placenta previa
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evidence of ruptured membranes up to delivery of infant
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Woman's Hospital
🇺🇸Baton Rouge, Louisiana, United States