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

H

Hadassah Medical Center

Status

Unknown

Conditions

Color Reaction With Amniotic Fluid

Treatments

Device: A disposable pad containing sensitive chemical indicators

Study type

Observational

Funder types

Other

Identifiers

NCT01022814
Momteclife-HMO-CTIL

Details and patient eligibility

About

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.

Enrollment

300 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • None.

Trial design

300 participants in 1 patient group

Pregnant woman
Treatment:
Device: A disposable pad containing sensitive chemical indicators

Trial contacts and locations

1

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Central trial contact

Nili Yanai, Dr'

Data sourced from clinicaltrials.gov

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