Expired Study
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New York, New York 10032


Purpose:

The aim of this study is to see whether a new self-sampling device, the Delphi Screener (Delphi Devices, Scherpenzeel, Netherlands), can be used for cervical cancer screening. The results using the new device will be compared to results using the current gold standard. The gold standard is clinician-collected endo-cervical and ecto-cervical specimens (often referred to as a 'Pap smear'). Additionally, women will be asked about the acceptability of using the device and how easy it is to understand the user instructions. The Delphi Screener is a sterile, plastic, syringe-like device containing buffered saline which allows a woman to collect her own vaginal lavage (to 'self-squirt'). The hypothesis is that the device may work well for cervical cytology and will be acceptable to the women in the study.


Criteria:

Inclusion Criteria: - Valid Pap smear in last 1-3 months obtained at participating clinic - 18 years or older - Self-report being able to read in English and/or Spanish - Willing to sign informed consent Exclusion Criteria: - Used vaginal product (douche, spermicide, antifungal) in last 48 hours - Last menses started ≤ 4 days prior to enrollment visit - No uterus / history of hysterectomy - Self-report currently pregnant - Self-report currently breastfeeding


NCT ID:

NCT00702208


Primary Contact:

Principal Investigator
Carolyn Westhoff, MD
Columbia University


Backup Contact:

N/A


Location Contact:

New York, New York 10032
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 16, 2018

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