Clinical Trials Logo

Clinical Trial 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


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Evidence of Ruptured Membranes in Women Greater Than 15 Weekd
  • Rupture

NCT number NCT02208011
Study type Observational
Source Louisiana State University, Baton Rouge
Contact
Status Completed
Phase
Start date August 2014
Completion date June 2015