- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03083249
Gardasil Knowledge
June 4, 2018 updated by: Sarah Hostetter, MD
Gardasil Anonymous Survey
Human papillomavirus (HPV) is the most common viral genital tract infection.
The majority of women and men who are sexually active will be exposed to a strain or strains of the virus.
While there are hundreds of viral strains, high risk strains are associated cervical and oral cancers.
According to the Centers for Disease Control (CDC), between 2008 and 2012 there were 38,793 deaths attributed to HPV related cancers.
Vaccinations were created in an attempt to prevent infection from the most common high risks strains of HPV.
Gardasil/HPV-9 was created to help prevent HPV related cancers and warts.
The HPV-9 vaccine includes protection from 7 strains of HPV associated with 74% of HPV related cancers.
While Gardasil was approved and released in 2006, many men and women have not been vaccinated.
A national immunization survey in 2011 of teens 13-17 years old noted that only 60% of girls and 40% of boys have received at least one vaccination in the series.
While complete vaccination series is recommended, a recent study found that a single dose of Gardasil when compared to placebo created a higher level of serum antibodies in uninfected females.
Study Overview
Detailed Description
All patients seen at a single clinic will be offered participation in the anonymous survey.
The survey will ask a series of questions regarding basic demographics, sexual history, smoking status, and Gardasil vaccine knowledge.
The survey will serve as evidence of the vaccine utility by highlighting patient risk factors for HPV and patient knowledge about the vaccine series.
Study Type
Observational
Enrollment (Actual)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Missouri
-
Saint Louis, Missouri, United States, 63117
- St. Mary's Health Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 26 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Females age 18-26 of all ethnic background
Description
Inclusion Criteria:
- All patients 18-26 will be offered participation
Exclusion Criteria:
- Not meeting the inclusion criteria
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
knowledge about HPV risk factors
Time Frame: 1 year
|
The survey asks about Gardasil vaccine knowledge
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Sarah Hostetter, MD, St. Louis University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2017
Primary Completion (Actual)
May 1, 2018
Study Completion (Actual)
June 1, 2018
Study Registration Dates
First Submitted
March 3, 2017
First Submitted That Met QC Criteria
March 13, 2017
First Posted (Actual)
March 17, 2017
Study Record Updates
Last Update Posted (Actual)
June 6, 2018
Last Update Submitted That Met QC Criteria
June 4, 2018
Last Verified
June 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 27816
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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