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Human Immunodeficiency Virus clinical trials

View clinical trials related to Human Immunodeficiency Virus.

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NCT ID: NCT01734850 Completed - Clinical trials for Human Immunodeficiency Virus

Safety Study of a Dual Anti-HIV Gene Transfer Construct to Treat HIV-1 Infection

Start date: April 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This is an early phase research study looking at whether an experimental gene transfer, LVsh5/C46 (also known as Cal-1), is safe and if it can protect the immune system from the effects of HIV without the use of antiretroviral drugs. Cal-1 is an experimental gene transfer agent designed to inhibit HIV infection through 2 active parts: 1. Removing a protein named CCR5 from bone marrow and white blood cells 2. Producing a protein named C46 on bone marrow and white blood cells

NCT ID: NCT01721226 Completed - Clinical trials for Human Immunodeficiency Virus

CARE Corrections: Technology for Jail HIV/HCV Testing, Linkage, and Care (TLC)

CARE+
Start date: August 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether an intervention (CARE+ Corrections) delivered to HIV-infected detainees within the DC Department of Corrections (DOC) and recently -released ex-detainees in the community can improve linkage to community HIV care and adherence to HIV medications after release, and ultimately achieve or maintain HIV viral suppression following community re-entry.

NCT ID: NCT01692236 Terminated - Clinical trials for Human Immunodeficiency Virus

Brain Imaging for HIV-Associated Thinking and Mood Disorders

Start date: September 13, 2012
Phase:
Study type: Observational

Background: - Human immunodeficiency virus (HIV) infection appears to cause problems with blood vessel function. These problems may add to some thinking and mood disorders found in people with HIV infection. Researchers want to evaluate HIV infected patients to see if blood vessel function contributes to thinking and mood disorders, such as early dementia and depression. To do so, they will compare study results between people with and people without HIV infection. Objectives: - To compare the thickness of blood vessel walls between people with and without HIV infection. - To study the relationship between blood vessel thickness and thinking and mood disorders. Eligibility: - Individuals between 25 and 55 years of age who have HIV infection. - Healthy individuals between 25 and 55 years of age. Design: - Participants will be screened with a physical exam and medical history. Blood and urine samples will be collected. - Participants will have imaging studies of the brain and major blood vessels in the head and neck. - Participants will also have neuropsychological testing. These tests will look at memory, learning and thinking ability, attention, and mood. - Participants will have the option of coming back for repeat blood tests every six months and repeat imaging studies and neuropsychological tests every year, over 1- 4 years period.

NCT ID: NCT01673750 Completed - HIV Clinical Trials

Body Image in Youth With HIV

Start date: October 2012
Phase: N/A
Study type: Observational

This is an observational study that seeks to gather information about perceptions of body image through the use of a one-time questionnaire completed by participants at the time of study enrollment. Effective management of Human Acquired Immune Deficiency Syndrome (AIDS) caused by the Human Immunodeficiency Virus (HIV) has become possible through the use of Highly Active Antiretroviral Treatment (HAART). As a result of more successful treatment options, HIV/AIDS has transitioned from a terminal illness to one which is treated as a chronic condition. One particular group that has been impacted tremendously by HIV in the United States is the adolescent population. As youth are living longer with HIV/AIDS, clinicians and researchers are beginning to examine ways in which the disease can affect one's physical health, mental health, and other psychosocial factors. Research emerging involving adults with HIV/AIDS has suggested that increased attention to and negative views of one's body image may be found at a higher rate in this group. To our knowledge, very few studies have examined this relationship in adolescents with HIV.

NCT ID: NCT01667731 Completed - Hepatitis C Clinical Trials

Efficacy and Safety of Sofosbuvir Plus Ribavirin in Chronic Genotype 1, 2 and 3 Hepatitis C Virus (HCV) and Human Immunodeficiency Virus (HIV) Co-infected Adults

Start date: July 2012
Phase: Phase 3
Study type: Interventional

This study will evaluate the efficacy, safety, and tolerability of sofosbuvir (SOF; GS-7977) plus ribavirin (RBV) in adults with chronic genotypes 1, 2, and 3 HCV infection who are coinfected with HIV-1.

NCT ID: NCT01666990 Recruiting - Clinical trials for Human Immunodeficiency Virus

Tripterygium Wilfordii Hook F (TwHF) Treatment for Immune Non-responders With HIV-1 Infection

Start date: June 2012
Phase: Phase 1/Phase 2
Study type: Interventional

HIV-1 infection is characterized by progressive depletion of CD4+ T cells that eventually leads to clinically significant immunodeficiency. A chronic generalized immune activation is now being recognized to be the main driving force for T cell depletion, loss of anti-HIV-1 immunity and disease progression during chronic HIV-1 infection. However, it is still unknown whether reducing immune activation will restore CD4 T cell counts and leading to immune reconstitution in chronic HIV infection. Tripterygium Wilfordii Hook F (TwHF) has been demonstrated to decrease immune activation of the host, and can suppress inflammation in human diseases. Here, the investigators propose a hypothesis that TwHF can reduce immune over-activation which subsequently leads to the restoration of CD4 T-cell counts and immune reconstitution in HIV-infected immune non-responders.

NCT ID: NCT01638312 Completed - Clinical trials for Human Immunodeficiency Virus

Development of Method of Fructose Identification in Urine to Detect the Viral Infection

Start date: June 2011
Phase: N/A
Study type: Observational

The goal of this research is the attempt to implement a new research method based on modern electrochemistry successes, in particular the development of the polarographic method of fructose and fructose diphosphate identification and its implementation to detect the viral infection in early stage. There will be 20 samples from the HIV-infected patients and 30 samples from the heath controls. The study will collect 10ml urine and examined fructose and fructose-diphosphate using the polarographic method.

NCT ID: NCT01616823 Completed - HIV Clinical Trials

Fetal HIV Transmission Risk and Duration of Membrane Rupture

Start date: January 2009
Phase:
Study type: Observational

In optimally managed HIV+ women with undetectable viral loads, who are on HAART and also receiving intrapartum IV ZDV, the risk of vertical transmission of HIV is independent of the length of time of rupture of membranes.

NCT ID: NCT01613157 Completed - Clinical trials for Human Immunodeficiency Virus

Predictors of Antiretroviral Pharmacokinetics in HIV-infected Women With Virologic Suppression

Start date: January 2006
Phase: N/A
Study type: Observational

The investigators would like to carry out this study to measure drug levels in HIV-infected women that are taking anti-HIV medications. This study will determine the predictors of high drug levels and will assess the association of drug levels and adverse events in women.

NCT ID: NCT01599364 Completed - Clinical trials for Human Immunodeficiency Virus

Atazanavir/r + Lamivudine Dual Therapy

ATLAS
Start date: April 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the virological efficacy of maintenance therapy with atazanavir with ritonavir combined with lamivudine in treatment experienced HIV positive patients with full and stable virological suppression.