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

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