A Comparison of Rapid Immunoassays for the Detection of Ruptured Membranes

Completed

Conditions studied: Evidence of Ruptured Membranes in Women Greater Than 15 Weekd

In brief

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

Key facts

Study ID
NCT02208011
Run by
Louisiana State University, Baton Rouge
People needed
140
Starts
2014-08-01
Expected to finish
2015-06-01
Last updated by the study team
2020-09-02

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.