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Human Papillomavirus (HPV) or Pap Examination (HOPE) Study

Complete title: Cytology vs. at home HPV screening for detection of CIN 2,3,CIS

Research Study Number       7489
    
Principal Investigator       Nancy Kiviat, MD
    
Phase       NA

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Research Study Description

This randomized clinical trial studies home-based HPV or clinic-based Pap screening for cervical cancer. It is not yet known whether home-based screening is more effective, cost-effective, and/or acceptable than clinic-based screening for cervical cancer.

Eligibility Criteria (must meet the following to participate in this study)

Ages Eligible for Study: 21 Years and older

Genders Eligible for Study: Female

- Able to provide informed consent in English

Other eligibility criteria may apply.

Exclusions (conditions that would prevent participation in this study)

- Have had hysterectomy

- Currently pregnant

- Received treatment of cervical dysplasia with loop electrosurgical excision procedure (LEEP), cone biopsy, laser procedure or cryotherapy within THREE years

- Received colposcopy of cervix within TWO years

- Received Pap test within ONE year

- Immunocompromised (positive human immunodeficiency virus [HIV] test, transplant recipient, received chemotherapy for cancer, or taking immunosuppressant drugs)

- Decisionally impaired adults requiring a legally authorized representative

Other exclusion criteria may apply.



Research Study Number       7489
    
Contact       John Lin
    
Telephone       206/616-8526
    
   

Keywords
Cervical Cancer; Gynecological Cancer; Solid Tumors; Uterine Cancer

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Please remember:

  • Talk to your health care providers first before making decisions about your health care.
  • Whether you are eligible for a research study depends on many things. There are specific requirements to be in research studies. These requirements are different for each study.

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