Performance Evaluation Study for Clearblue Pregnancy Test
- Conditions
- Pregnancy
- Registration Number
- NCT01077583
- Lead Sponsor
- SPD Development Company Limited
- Brief Summary
The purpose of this study is to collect urine samples and dating scan information from women who wish to become pregnant. Urine samples will be tested in the laboratory with the Clearblue Pregnancy Test and the results correlated with volunteer information.
- Detailed Description
Approximately 800 female volunteers wishing to become pregnant will be recruited locally around 5 trial centers within the US.
Daily urine samples and gestational age dating scan information obtained from the study will be used in laboratory tests to assess the accuracy of the Clearblue Pregnancy Test. Product assessment will involve testing of early morning urine samples collected by women during the cycle in which they conceived. Urine samples will be collected pre-conception to the end of the second trimester.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 800
- Provide written informed consent to participate in the study and agree to comply with study procedures.
- Has menstrual bleeds.
- Seeking to become pregnant.
- Intend to seek medical care during pregnancy.
- Has positive pregnancy test on screening.
- Has received medical treatment for infertility or is participating in an assisted fertility program.
- Known condition to contra-indicate pregnancy.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The agreement of the Clearblue Pregnancy Test result with Duration of Pregnancy. 1 year
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
Radiant Research Inc
🇺🇸San Antonio, Texas, United States
Radiant Research, Inc.
🇺🇸Chicago, Illinois, United States