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NCT00710593 · ClinicalTrials.gov registry record · Phase 2

Impact of a Human Papilloma Virus (HPV) Vaccine in HIV-Infected Young Women

A Phase 2 study of HIV Infection, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
Phase 2
Development phase
99
Enrollment target
14
Study locations

NCT00710593 is a Phase 2 study of HIV Infection that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 99 participants, below the 241-participant average among 73 other HIV Infection trials with a reported enrollment target (59% lower). The trial reports 14 study locations across 10 states.

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The verdict

NCT00710593, a Phase 2 study of HIV Infection, has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
Phase 2
Development phase
99 participants
Enrollment target
14
Study locations

Study Summary

The purpose of this study is to evaluate the immunogenicity, safety, tolerability, and behavioral impact of an HPV-6, -11, -16, -18 vaccine in HIV-infected young women.

Conditions Studied

Interventions

  • BIOLOGICAL HPV vaccine for strains -6, -11, -16, and -18

Study Locations (14)

Florida

  • Childrens Diagnostic & Treatment Center - Fort Lauderdale
  • University of Miami School of Medicine - Miami
  • USF College of Medicine - Tampa

Illinois

  • Ruth M Rothstein CORE Center/ John H Stroger Jr Hospital - Chicago
  • Childrens Memorial Hospital - Chicago

New York

  • Mount Sinai Medical Center - New York
  • Montefiore Medical Center - The Bronx

California

  • Childrens Hospital of Los Angeles - Los Angeles

District of Columbia

  • Childrens National Medical Center - Washington D.C.

Louisiana

  • Tulane University Health Sciences Center - New Orleans

Maryland

  • University of Maryland - Baltimore

Pennsylvania

  • Childrens Hospital of Philadelphia - Philadelphia

Trial Details

FieldValue
Enrollment Target 99 participants
Start Date 2008-02
Est. Completion 2011-02
Phase Phase 2

What the Registry Record Tells You About NCT00710593

The ClinicalTrials.gov registry entry for NCT00710593 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 99 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 241-participant average among 73 other HIV Infection trials with a reported enrollment target (59% lower). The listed sponsor is University of North Carolina, Chapel Hill, which has 1,109 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with HIV Infection appearing as the primary indexed condition, and to 1 intervention - of which HPV vaccine for strains -6, -11, -16, and -18 is the first listed.

NCT00710593 reports 14 study locations spanning 10 distinct geographic areas - top geographies include Florida, Illinois, New York.

Frequently Asked Questions

What is clinical trial NCT00710593 about?

NCT00710593 is a clinical study titled "Impact of a Human Papilloma Virus (HPV) Vaccine in HIV-Infected Young Women". The purpose of this study is to evaluate the immunogenicity, safety, tolerability, and behavioral impact of an HPV-6, -11, -16, -18 vaccine in HIV-infected young women.

What is the current status of trial NCT00710593?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 99 participants. The study started on 2008-02. Estimated completion is 2011-02.

What conditions does trial NCT00710593 study?

This clinical trial studies the following conditions: HIV Infection.

What interventions are being tested in trial NCT00710593?

The interventions under investigation include: HPV vaccine for strains -6, -11, -16, and -18 (BIOLOGICAL).

Who is sponsoring clinical trial NCT00710593?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00710593 being conducted?

This trial has 14 study locations across California, District of Columbia, Florida, Illinois, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.