Skip to main content
Clinical Trials/NCT01022814
NCT01022814UnknownNot Applicable

Development of a Diagnostic Device for Identifying Between Amniotic Fluid to Urine

Hadassah Medical Organization1 site in 1 country300 target enrollmentStarted: January 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
300
Locations
1

Study Overview

Brief Summary

In the final months of pregnancy, women need to know whether their 'water is broken' necessitating a race to the delivery room, or whether pressure of the foetus on their bladder has caused them merely to pass urine. They may also have faced the same dilemma on many occasions much earlier in the pregnancy. With this development the investigators will provide them with an immediate answer to this critical question.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Cross Sectional

Eligibility Criteria

Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Amniotic fluid that were taken after the 17th week.

Exclusion Criteria

  • Not provided

Investigators

Sponsor Class
Other

Study Sites (1)

Loading locations...

Similar Trials