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HIV Infections clinical trials

View clinical trials related to HIV Infections.

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NCT ID: NCT00183573 Completed - HIV Infections Clinical Trials

HIV Prevention Program for Patients Receiving Care at a Sexually Transmitted Diseases Clinic

Start date: March 2004
Phase: Phase 2/Phase 3
Study type: Interventional

This study will determine the effectiveness of a two-step HIV prevention program in reducing risky sexual practices and decreasing the incidence of sexually transmitted diseases (STDs).

NCT ID: NCT00183456 Completed - HIV Infections Clinical Trials

A Peer-Oriented HIV Prevention Outreach Program for Individuals at High Risk for HIV and Other STIs

Start date: September 2005
Phase: Phase 2
Study type: Interventional

This study will determine the effectiveness of a peer outreach intervention in preventing HIV infection in adults at high risk for contracting HIV and other sexually transmitted diseases (STDs).

NCT ID: NCT00183287 Completed - HIV Infections Clinical Trials

Long Term Follow-Up of HIV Infected Patients Who Have Previously Participated in HIV Clinical Trials

Start date: n/a
Phase:
Study type: Observational

The purpose of this study is to monitor the progression of HIV infection and HIV-related disease processes in patients who have previously participated in HIV clinical trials.

NCT ID: NCT00183261 Completed - HIV Infections Clinical Trials

Immune Response to a Therapeutic HIV Vaccine Followed by Treatment Interruption in Patients With Acute or Recent HIV Infection

Start date: March 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the HIV vaccine MRKAd5 HIV-1 gag/pol/nef followed by treatment interruption can increase immune system function in adults with acute or recent HIV infection who have started taking anti-HIV drugs.

NCT ID: NCT00179335 Completed - HIV Infections Clinical Trials

Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Between Older and Younger HIV-Infected Adults

Start date: August 2003
Phase:
Study type: Observational

HIV infected patients, aged </= 35 years and aged >/= 55 years, who are regularly taking either efavirenz (EFV) or lopinavir/ritonavir (Lop/r) as part of their antiretroviral regimen are being asked to spend 12 hours at the researchers' clinic (the ACS clinic at Jacobi Medical Center, Bronx, New York) for an intensive pharmacokinetic study in which 5 cc of blood will be drawn 9 times over a 12 hour period. Patients taking EFV will return for one additional blood draw the following day.

NCT ID: NCT00173329 Recruiting - HIV Infections Clinical Trials

The Quality of Life of Patients With Severe Illnesses

Start date: August 2005
Phase: Phase 2
Study type: Observational

Lately researchers and clinicians have emphasized the health related quality of life. Several reasons account for this trend. First of all, the advanced medical practices have contributed to the increased life expectancy. Secondly, the pattern of diseases has shifted from high acuity to chronicity. Therefore, the effectiveness of health care could not be solely evaluated by the rates of morbidity and mortality. The state of patients’ quality of life has become the pivotal indicator of the effectiveness of health care interventions. On the other hand, patients’ subjective perceptions of health care are crucial factors in treatment processes. Therefore quality of life becomes reference in choosing health care interventions to enhance the benefits of patients. The scopes of quality of life research include the essence of quality of life, the measurements of quality of life and the relationships between quality of life and its related factors, etc. The local researchers have long put efforts in quality of life research. The results of these studies have contributed to the understandings of different patients’ quality of life. However, the majority of studies have focused on specific diseases. This study propose to extend the scope of quality of life research to study patients’ quality of life of two severe illnesses, i.e. HIV infections and schizophrenia. These two illnesses represent two severe physical and psychiatric illnesses. Even their etiology, mechanisms, disease process, signs and symptoms, and treatments are different. However, the similarities of these two illnesses include both are severe illnesses without cure, both are stigmatized by the society. Patients with these two illnesses suffer in their personal lives, social relations and quality of life. Therefore the current study to further investigate and compare and contrast the essence of patients’ quality of life and their related factors. The proposed study is a second year study of the two-year study - The quality of life of patients with severe illnesses (NSC93-2314-B-002-294). The first year study focused on the investigation of the quality of life of patients with HIV infections (NSC93-2314-B-002-294). The aim of this proposed study is to compare and contrast the quality of life and its related factors of patients with schizophrenia and HIV infections. The contributions of this study include the in-depth understandings of quality of life of patients with HIV infections and schizophrenia and the comparison of quality of life of different illnesses. The results serve as the foundations in future development of intervention programs to enhance patients’ quality of life and cost-effectiveness analyses.

NCT ID: NCT00172315 Recruiting - Clinical trials for Acquired Immunodeficiency Syndrome

Proton Magnetic Resonance Spectroscopy (1H MRS) in Evaluating the Bone Marrow, Muscle and Adipose Tissue on Normal and Human Immunodeficiency Virus Infected Subjects

Start date: December 2003
Phase: Phase 3
Study type: Observational

Magnetic resonance spectroscopy (MRS) is commonly applied in medicine with 1H proton or 31-phosphorus spectra. The proton MRS is often used in evaluating the central nervous system and 31P MRS is used in muscular diseases or neoplasms. However, the proton MRS is also considered to be applied to the musculoskeletal system because of its profound amount of protons. Ballon used the STEAM technique, and Schick used the PRESS technique, to investigate the lipid and water spectra of the bone marrow and also correlated those with hematological diseases and post-treatment effects. Schellinger et al. used the STEAM sequence to calculate the lipid content of the vertebral bone marrow and found that it was influenced according to age and sex. The investigator had used the proton MRS to evaluate the lipid and water spectra of the femoral head and revealed its significance in predicting avascular necrosis of the femoral head. According to the above research literature, the investigators considered further investigation of the proton MRS in evaluating the musculoskeletal system.

NCT ID: NCT00168246 Active, not recruiting - HIV Infections Clinical Trials

Determining the Prevalence of HIV-Related Neurological Disorders in the Asia Pacific

Start date: June 2005
Phase: N/A
Study type: Observational

This study will determine the prevalence of HIV-related neurological disorders in the countries of the Asia-Pacific Region.

NCT ID: NCT00168233 Completed - HIV Infections Clinical Trials

Impact of HIV and Its Treatment on Reverse Cholesterol Transport

Start date: June 2005
Phase: N/A
Study type: Observational

To investigate the effect of treatment of HIV infection with highly active antiretroviral therapy on individual steps of reverse cholesterol transport, endothelial function and intima-media thickness in HIV patients.

NCT ID: NCT00168220 Withdrawn - HIV Infections Clinical Trials

Predictors of Drug Hypersensitivity in HIV Infected Subjects

Start date: August 2005
Phase: N/A
Study type: Observational

A case-control study to look at hypersensitive and tolerant individuals matched for HLA genetic predisposition, when considering predictors of drug hypersensitivity.The study aims to identify the immunological factors increasing the risk of drug reactions in HIV positive individuals.