The Human Papillomavirus (HPV) Transmission Pilot Study

NCT ID: NCT00823511

Last Updated: 2015-01-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

137 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-10-31

Study Completion Date

2014-12-31

Brief Summary

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This transmission pilot study is a prospective study to determine feasibility of enrolling female partners into an international transmission study. Companion study to MCC-13930.

Detailed Description

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We planned to enroll 150 female sexual partners, 75 per year for 2 years, of male study participants in the HPV Infection in Men (HIM) Study. The enrollment period is from June 2006 through May 2008 and participants will be followed through May 2010. At all study visits participants will undergo interviews, a physical exam and laboratory analysis for HPV for a total of 5 clinical visits scheduled every 6 months over 2 years of follow-up. In addition, at each study visit, participants will provide blood for HPV antibody analyses. At enrollment, visit 3 and visit 5 a Pap smear test will be done. At the enrollment visit, study participants will complete a questionnaire designed to assess social and behavioral risk factors for the acquisition of HPV. At each subsequent study visit, participants will be asked to provide updated information to assess changes in risk behaviors such as condom use, relations with new partners, and tobacco use.

Conditions

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Human Papillomavirus Infection

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Female Partners

Female partners of HIM Study participants

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Female partners of HIM Study participants
* report no abnormal Pap smear during the past 6 months;
* have not had a hysterectomy
* have never been diagnosed with genital warts;
* are not pregnant;
* residents of southern Florida;
* are not and have not been enrolled in an HPV vaccine trial;
* willing to comply with scheduled visits every 6 months for 2 years.
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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H. Lee Moffitt Cancer Center and Research Institute

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Anna Giuliano

Role: PRINCIPAL_INVESTIGATOR

H. Lee Moffitt Cancer Center and Research Institute

Locations

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Moffitt Cancer Center & Research Institute

Tampa, Florida, United States

Site Status

Countries

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United States

Other Identifiers

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USF IRB 104923

Identifier Type: -

Identifier Source: secondary_id

MCC-14881

Identifier Type: -

Identifier Source: org_study_id

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