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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00021775
Other study ID # HPTN 033
Secondary ID 10611
Status Completed
Phase N/A
First received August 4, 2001
Last updated December 31, 2013
Start date April 2002
Est. completion date February 2004

Study information

Verified date December 2013
Source National Institute of Allergy and Infectious Diseases (NIAID)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

The purpose of this study is to set up a system for doing research on HIV prevention in various parts of the world.

In order to plan large, long-term studies on the prevention of HIV in different areas of the world, it is necessary to get certain information first. It is important to know about the rate of HIV infection and how to get people to enroll for any future studies. This study will be done at 4 study locations.


Description:

In order to realistically plan for future Phase III studies on HIV prevention, information must be obtained to characterize study population parameters at HTPN sites. Very different study designs may be required depending on these parameters, such as the ability of HPTN research centers to recruit study participants and the rate of HIV incidence observed in study populations. This study will be conducted at 4 HPTN sites to establish the necessary research knowledge and infrastructure.

This study enrolls participants from St. Petersburg, Russia; Xinjiang and Guangxi, China; and Chennai, India who are at high risk for HIV infection due to sexual and/or drug use behaviors. Participants who meet the screening criteria then complete an HIV risk assessment interview, receive HIV pre-test and risk reduction counseling, and undergo phlebotomy for HIV antibody testing. Participants who test positive are referred to available services and studies. Those who test HIV-negative and meet eligibility criteria are enrolled and maintained in follow-up over the next 12 months. Participants complete "locator contacts" at Months 3 and 9 and have follow-up visits at Months 6 and 12 for similar tests as performed at entry. In a substudy of this trial in China, participants will be interviewed about their drug use, social networks, needs, and perceptions about HIV/AIDS. These results will be used by HPTN to design more culturally sensitive and appropriate trials in the future.


Recruitment information / eligibility

Status Completed
Enrollment 2000
Est. completion date February 2004
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 14 Years and older
Eligibility Inclusion Criteria

Participants may be eligible for this study if they:

- Are 16 (Saint Petersburg) or 18 (Xinjiang, Guangxi, and Chennai) years of age or older.

- Are HIV sero-negative.

- Are available for 12 months of study participation.

- Have written consent of parent or legal guardian if under age.

- Are able and willing to provide information on where they can be located or contacted.

- Meet specific risk-group requirements, for women at heterosexual risk, for men at heterosexual risk, and for injection drug users.

Exclusion Criteria

Participants will not be eligible for this study if they:

- Have any mental disorders that would cause a problem with the informed consent or study participation.

- Have any condition that, in the opinion of the doctor, would interfere with the study.

Study Design

N/A


Related Conditions & MeSH terms


Locations

Country Name City State
China Guangxi Ctrs. for Disease Control & Prevention and for HIV/AIDS Prevention & Control CRS Nanning Guangxi
China Xinjiang Uygar Autonomous Region Ctr. for Disease Control & Prevention, HPTN Project Office Urumqi Xinjiang
Russian Federation St. Petersburg Univ. Biomedical Ctr. St. Petersburg

Sponsors (4)

Lead Sponsor Collaborator
National Institute of Allergy and Infectious Diseases (NIAID) Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institute of Mental Health (NIMH), National Institute on Drug Abuse (NIDA)

Countries where clinical trial is conducted

China,  Russian Federation, 

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