View Clinical Trial (Medical Research Study)
A Model for Implementation of Cervical Cancer Screening and HPV Vaccination the Emergency Department: a Pilot Study - NCT01133509-23507(Clinical Trial 651775)
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Norfolk |
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State:
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VA |
| Zip Code: |
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23507 |
| Conditions: |
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Human Papillomavirus (HPV) |
| Purpose: |
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In this pilot study, we intend to demonstrate that a great portion of women at high risk
(inadequate screening, HPV 16/18 and/or cytology) are presenting to the ED, cytology/ HPV
testing via ThinPrep®Pap testTM and surveillance. We intend to provide improved access to
healthcare and monitoring through administration of vaccine to eligible patients and 1 year
follow up for patients involved in this study.
Females meeting inclusion/exclusion criteria participating in the study (n=100) that have
not had a cytology test in 2 or more years will be offered the Thin Prep® cytology test.
This study will allow surveillance of disease through cytology and HPV DNA testing via
collection of data using Thin Prep® cytology with reflex HPV DNA testing according to
established guidelines as described below.
Provide improved access to healthcare and monitoring through administration of vaccine for
eligible females as established by guidelines. Patients will receive first vaccine in the
ED and will have arranged follow up for administration of the 2 month and 6 month series of
the HPV vaccination. Through data collection, we intend to determine if there is a need for
vaccination and determine if patients are likely to follow up..
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- 3 years of beginning sexual activity or by age 21 years whichever occur first.
- resident of the City of Norfolk, Virginia
- uninsured
Exclusion Criteria:
- Pregnant women
- Women with Hysterectomy with cervical excision
- Women who received full HPV vaccine series
- Known history of cervical cancer
- Male sex
- Loop electrocautery excision procedure(LEEP)
- Cold-Knife conization |
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| Study is available at: |
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Sentara Norfolk General Hospital Norfolk, VA 23507 United States
Primary Contact: Alicia Devine, MD Email: aliciadevine@mac.com Phone: 757-388-3397 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 23, 2011 |
Modifications to
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