A Comparison of Rapid Immunoassay Tests for the Detection of Ruptured Membranes

NCT01668472 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2013-12-23

No results posted yet for this study

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.

Conditions

  • Pregnant Woman With Premature Rupture of Amnion Membranes

Sponsors & Collaborators

  • University of Colombo

    lead OTHER

Principal Investigators

  • Dr. M. Rajapaksha, MD · De Soysa Maternity Hospital, Kynsey Road, Colombo 08, Sri Lanka

Eligibility

Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2013-08-31
Completion
2013-12-31

Countries

  • Sri Lanka

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01668472 on ClinicalTrials.gov