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A Model for the Implementation of the Cervical Cancer Screening and HPV Vaccination in the Emergency Department: a Pilot Study.


N/A
18 Years
26 Years
Open (Enrolling)
Female
Genital Human Papilloma Virus Infection

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Trial Information

A Model for the Implementation of the Cervical Cancer Screening and HPV Vaccination in the Emergency Department: a Pilot Study.


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

Type of Study:

Interventional

Study Design:

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

To demonstrate that a great portion of women at high risk (inadequate screening, HPV 16/18 and /or cytology)are presenting to the ED,by analysis of a constructed survey,cytology/HPV testing via ThinPrep Pap test and surveillance

Outcome Time Frame:

two years

Safety Issue:

No

Principal Investigator

Alicia Devine, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Eastern Virginia Medical School

Authority:

United States: Institutional Review Board

Study ID:

33249

NCT ID:

NCT01133509

Start Date:

September 2009

Completion Date:

October 2012

Related Keywords:

  • Genital Human Papilloma Virus Infection
  • Uterine Cervical Neoplasms
  • Emergencies
  • Papilloma
  • Virus Diseases
  • Warts
  • Papillomavirus Infections

Name

Location

Sentara Norfolk General HospitalNorfolk, Virginia  23507