CClinicalTrials.gg
CompletedNCT00711815Updated Aug 5, 2011

A Study to Identify Markers in Blood and Tissue of HPV Clearance

An observational study in HPV Infections, sponsored by University of Alabama at Birmingham. Completed at 1 site in United States. Open to female participants aged 19 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-08-05.

Sponsored by University of Alabama at Birmingham · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
197
Ages
19 Years and older
Sex
Female
01

Study summary

This is a research study looking at gene characteristics in blood and Pap smear samples in hopes of identifying markers that will predict if the HPV infection is present or not.

Read the detailed description

Because infection with high-risk human papillomavirus is a necessary cause of cervical cancer, HPV testing has many potential uses in cervical cancer screening. Unfortunately, like cytology, it suffers from a lack of specificity when used for population-based screening. Given that HPV testing detects more cases of CIN3+ than cytology and that it would probably be more practical in developing regions, finding a biomarker that would increase specificity has been the goal for much research on HPV and cervical cancer. The goal of this study is to explore potential predictors of viral clearance, specifically RNA levels of candidate genes in cervical swabs and host genetic polymorphisms, in the context of genotype-specific infection data.

02

Conditions studied

  • HPV Infections

Keywords

  • Women of the state of Alabama
  • CIN 1
  • negative biopsy
  • normal colposcopy
  • HPV
03

In context

Papillomavirus Infections

495 studies on the registry are indexed under Papillomavirus Infections; 125 are open to participants now.

This study's enrollment of 197 is below the median of 400 across 147 observational studies indexed under Papillomavirus Infections.

Browse Papillomavirus Infections studies →

Lead sponsor

University of Alabama at Birmingham is the lead sponsor of 1,396 studies on the registry; 284 are open to participants now.

Of its 156 completed or terminated interventional studies of FDA-regulated products, 124 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

HPV-positive women with biopsy-confirmed CIN 1 or negative biopsies or normal colposcopic findings

Inclusion criteria

  • HPV positive

Exclusion criteria

Exclusion Criteria:

  • Negative for HPV
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
197 participants (actual)
Biospecimen retention
Samples with dna

Groups and cohorts

  • UA

    HPV positive

06

Study locations

1 site
  • University of Alabama at Birmingham
    Birmingham, Alabama 35205, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 5, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00711815
Lead sponsor
University of Alabama at Birmingham
First posted
Jul 9, 2008
Start date
Jan 2007
Primary completion
Nov 2010
Completion
Nov 2010
Last update
Aug 5, 2011

Study contacts

Warner K Huh, M.D.
principal investigator · University of Alabama at Birmingham

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2011. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion