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A Study of Patients Who Recently Have Been Infected With HIV

Primary Purpose

HIV Infections

Status
Withdrawn
Phase
Locations
United States
Study Type
Observational
Intervention
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an observational trial for HIV Infections focused on measuring Virus Replication, HIV-1, Polymerase Chain Reaction, DNA, Viral, RNA, Viral, Sensitivity and Specificity, Anti-HIV Agents, Viral Load, Proviruses, Acute Infection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria Patients may be eligible for this study if they: Have had certain tests indicating that they recently have been infected with HIV. Agree to use effective methods of birth control during the study and for 3 months after. Are at least 18 years old. Exclusion Criteria Patients will not be eligible for this study if they: Have taken anti-HIV drugs. Take erythropoietin, G-CSF or GM-CSF within 30 days of study entry. Take interferons, interleukins, cytotoxic chemotherapy, or HIV vaccines within 30 days of study entry. Take medications that should not be taken with their prescribed anti-HIV drugs. Have had radiation treatment within 30 days of study entry. Are pregnant or breast-feeding.

Sites / Locations

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
October 19, 2000
Last Updated
March 5, 2015
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT00006415
Brief Title
A Study of Patients Who Recently Have Been Infected With HIV
Official Title
Evaluation of Subjects With Primary or Early Human Immunodeficiency Virus (HIV) Infection
Study Type
Observational

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Withdrawn
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to find out if anti-HIV drugs, taken by patients who are newly infected with HIV, can make the level of HIV in the body too low to detect. Studying patients who recently have been infected with HIV may help researchers understand how HIV infection works and how anti-HIV drugs may help these patients. Approved anti-HIV drugs can reduce the amount of HIV, but more research needs to be done in newly infected patients. This study will look at recently HIV-infected patients to study the progression of HIV disease and to see whether anti-HIV drugs can reduce the level of HIV.
Detailed Description
Primary and early HIV infection represents a potentially unique opportunity to better understand the pathogenesis of HIV infection, as well as to potentially prevent the establishment of latent infection. Approved antiretroviral therapy is able to reduce plasma viremia to unmeasurable levels in established infection and several groups have observed comparable effects in recently infected adults. This study is designed to evaluate and follow a cohort of patients with primary or early HIV infection and to evaluate the time course of latent infection and whether latent infection in CD4 cells will allow viral persistence despite antiretroviral therapy. Patients begin antiretroviral therapy within 7 days of enrollment. All patients are evaluated for treatment compliance and complete a compliance questionnaire regularly. Clinical evaluations, including CD4, CD8, and HIV RNA counts also are done regularly. Antiretroviral therapy is discontinued if there is no detectable virus by ultrasensitive assay and culture techniques in plasma, PBMCs, and lymphoid tissue. In a subset of patients, genital secretions and CSF (cerebrospinal fluid) are evaluated. If relapse occurs, antiretroviral therapy is re-instituted. In addition, virology and immunology substudies are performed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Virus Replication, HIV-1, Polymerase Chain Reaction, DNA, Viral, RNA, Viral, Sensitivity and Specificity, Anti-HIV Agents, Viral Load, Proviruses, Acute Infection

7. Study Design

Enrollment
0 (Actual)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients may be eligible for this study if they: Have had certain tests indicating that they recently have been infected with HIV. Agree to use effective methods of birth control during the study and for 3 months after. Are at least 18 years old. Exclusion Criteria Patients will not be eligible for this study if they: Have taken anti-HIV drugs. Take erythropoietin, G-CSF or GM-CSF within 30 days of study entry. Take interferons, interleukins, cytotoxic chemotherapy, or HIV vaccines within 30 days of study entry. Take medications that should not be taken with their prescribed anti-HIV drugs. Have had radiation treatment within 30 days of study entry. Are pregnant or breast-feeding.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Margaret Fischl
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Allan Rodriguez
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ernesto Scerpella
Official's Role
Study Chair
Facility Information:
City
Horsham
State/Province
Pennsylvania
ZIP/Postal Code
19044
Country
United States

12. IPD Sharing Statement

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A Study of Patients Who Recently Have Been Infected With HIV

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