Expired Study
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Detroit, Michigan 48201


Purpose:

The purpose of this study is to demonstrate that the Diagnostic Absorbent Panty liner (AL-SENSE Amniotic Leak Test Kit), developed by Common Sense Ltd., can distinguish between wetness sensed by pregnant women that is caused by amniotic fluid leakage and that which is caused by urinary incontinence.


Criteria:

Inclusion Criteria: - age 18 to 45 years. - minimum 16 weeks of pregnancy. - willing to sign the informed consent form. - arrived at the obstetric department reporting a feeling of vaginal wetness (undetermined whether this is amniotic fluid leakage or urinary incontinence). Exclusion Criteria: - experienced intermittent vaginal bleeding between the 2nd and 3rd trimester. - have had sexual relations within the last 12 hours. - unable or unwilling to cooperate with study procedures. - used the AL-SENSE before joining this study. - diagnosed with Bacterial Vaginosis or Trichomonas infection within the last 3 days. - uses vaginal products such as some douching formulas, some antibiotic treatments which reduce lactobacillus population. - uses drugs which reduce estrogen level such as tamoxifen or drugs that dry out the mucous membranes, such as antihistamines - on a diet of alkalizing foods such as Alkalive™ Green, which may cause elevation of the vaginal pH level.


NCT ID:

NCT00604838


Primary Contact:

Principal Investigator
Jacob Bornstein, MD
Western Galilee Hospital-Nahariya


Backup Contact:

N/A


Location Contact:

Detroit, Michigan 48201
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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