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HIV Infections clinical trials

View clinical trials related to HIV Infections.

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NCT ID: NCT00065104 Completed - HIV Infections Clinical Trials

Dehydroepiandrosterone Effects on HIV-1 Replication

Start date: October 2000
Phase: Phase 2
Study type: Interventional

This study's purpose is to learn how dehydroepiandrosterone (DHEA) affects the HIV virus, the immune system, hormone levels, body composition and quality of life.

NCT ID: NCT00064740 Completed - Clinical trials for Human Immunodeficiency Virus

Relaxation Response With Acupuncture for HIV Patients

Start date: July 2003
Phase: Phase 2
Study type: Interventional

Advances in treatment has turned HIV/AIDS into a chronic illness. Relaxation response is a state in which individuals evoke a bodily calm, effecting physiological changes that are shown to be associated with improved immune functioning. Acupuncture and relaxation are thought to both induce calm and deep relaxation in mind and body. This trial will study the combined effects of acupuncture and relaxation response in HIV patients.

NCT ID: NCT00064623 Completed - Pain Clinical Trials

Study of NGX-4010 for the Treatment of Painful HIV-Associated Neuropathy

Start date: August 2003
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine if an investigational drug, NGX-4010 (high-concentration capsaicin patch), is effective in treating painful HIV-associated neuropathy.

NCT ID: NCT00063804 Completed - HIV Infections Clinical Trials

Safety of AMD070 When Administered Alone or Boosted With Low-Dose Ritonavir in HIV Uninfected Men

Start date: n/a
Phase: Phase 1
Study type: Interventional

Most currently approved anti-HIV drugs work by stopping the replication of HIV after it has entered cells. AMD070 (also known as AMD11070) is designed to block HIV from entering cells and may be effective in treating patients who have developed resistance to or are unable to take other anti-HIV drugs. This study will evaluate the safety of different doses of AMD070 along with AMD070 boosted with ritonavir (RTV) in HIV uninfected men.

NCT ID: NCT00063778 Completed - HIV Infections Clinical Trials

Safety of an HIV Vaccine (AVX101) in HIV Uninfected Volunteers in the United States and South Africa

Start date: July 2003
Phase: Phase 1
Study type: Interventional

The purpose of this study is to see if different doses of an experimental HIV vaccine are safe and to study how the immune system responds to the vaccine. The vaccine will be tested in healthy, HIV uninfected volunteers. AVX101 contains only one of the many substances that HIV needs to make more copies of itself; therefore, the vaccine cannot cause HIV or AIDS.

NCT ID: NCT00062660 Approved for marketing - HIV Infections Clinical Trials

Tipranavir in Patients With Progressive, Systemic HIV-1 Disease Who Have Failed or Are Intolerant to Currently Approved Treatments for HIV Infection

Start date: May 2003
Phase: N/A
Study type: Expanded Access

To provide early access to tipranavir and evaluate the safety and tolerance of tipranavir combined with low dose of ritonavir in patients with progressive, HIV-1 disease who have failed or are intolerant to currently approved treatments for HIV infection, who are unable to participate in another tipranavir controlled clinical trial and have an urgent need for anti-HIV treatment.

NCT ID: NCT00062634 Recruiting - HIV Infections Clinical Trials

Education Program to Promote Female Condom Use

Start date: June 2003
Phase: N/A
Study type: Interventional

The female condom offers women a potentially important option for HIV prevention. This study will develop and evaluate a health education program to increase female condom use among ethnically diverse women.

NCT ID: NCT00062530 Not yet recruiting - HIV Infections Clinical Trials

Safety of an Oral HIV Vaccine in HIV Uninfected Volunteers

Start date: n/a
Phase: Phase 1
Study type: Interventional

This study will test the safety of and immune response to an oral HIV vaccine in healthy volunteers. The vaccine in this study uses a weakened bacterium called Salmonella typhi to deliver an HIV gene into the body through the mouth. The body then produces an HIV protein from the gene; this protein stimulates an anti-HIV immune response. The vaccine contains only one of the many substances that HIV needs to make more copies of itself, so the vaccine itself cannot cause HIV or AIDS.

NCT ID: NCT00061321 Completed - HIV Infections Clinical Trials

Daily Nevirapine to Prevent Mother to Infant Transmission of HIV

SWEN
Start date: August 2002
Phase: Phase 3
Study type: Interventional

Infants who are breast-fed by HIV infected mothers have an increased risk of becoming infected with HIV. Standard therapy for the prevention of HIV infections in infants included zidovudine (ZDV) prior to the onset of labor, a single dose of nevirapine (NVP) for women during labor, and a single dose of NVP for newborns given 72 hours after birth. This study will determine if giving low dose daily NVP to breastfed infants of HIV infected mothers, in addition to standard therapy, will be more effective than standard therapy alone at preventing HIV infections in these infants.

NCT ID: NCT00061256 Completed - HIV Infections Clinical Trials

The Effect of Alendronate, Calcium, and Vitamin D on Bone Mineral Density in HIV Infected Patients

Start date: n/a
Phase: Phase 2
Study type: Interventional

Alendronate is a drug that is used to treat osteoporosis. The purpose of this study is to examine whether alendronate in combination with calcium and vitamin D is safe and effective for treating bone loss in people with HIV.