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NCT ID: NCT00044902 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Monoclonal Antibody Treatment for Non-Hodgkin's Lymphoma (Low-Grade)

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

Epratuzumab is currently being studied in combination with rituximab, for the treatment of patients with low-grade NHL who failed previous chemotherapy and have never received rituximab or who received rituximab as a single agent or in combination with chemotherapy as their last treatment and who demonstrated a partial response or complete response for at least 12 months.

NCT ID: NCT00045864 Completed - Clinical trials for Lymphoma, Non-Hodgkin

Proleukin in Combination With Rituxan in Patients With Intermediate and High-Grade Non-Hodgkin's Lymphoma.

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

The purpose of this study is to determine the safety and effectiveness of combination therapy with Proleukin and Rituxan on patients with intermediate-and high- grade Non-Hodgkin's lymphoma.

NCT ID: NCT00045877 Completed - Clinical trials for Lymphoma, Non-Hodgkin

Proleukin in Combination With Rituxan in Patients With Low-Grade Non-Hodgkin's Lymphoma Who Have Previously Failed Rituxan Treatments

Start date: n/a
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine the safety and effectiveness of combination therapy with Proleukin and Rituxan on patients with low-grade Non-Hodgkin's Lymphoma who have previously failed Rituxan treatments.

NCT ID: NCT00046033 Completed - HIV Infections Clinical Trials

Comparing Standard-Dose Versus Adjusted-Dose Lopinavir/Ritonavir Therapy in HIV-Infected Persons With Drug Resistance

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

The purpose of this study is to see if adjusting the dose of lopinavir/ritonavir (LPV/r) has a better effect on lowering HIV viral load (the amount of HIV in the blood) compared to taking the standard FDA-approved LPV/r dose. This study will also compare the safety and tolerability of these two types of dosing.

NCT ID: NCT00046124 Completed - Clinical trials for Endocrine Dysfunction

Organophosphate Pesticides and Human Reproductive Health

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

This prospective cohort study assesses the effects of exposure to organophosphate (OP) pesticides on adverse reproductive outcomes in both male and female agricultural workers in China. We will enroll women and their spouses, who are attempting to become pregnant, and observe reproductive endpoints including (1) semen parameters (concentration, total count, motility, progression and morphology), (2) menstrual disorders (oligomenorrhea, amenorrhea, polymenorrhea, intermenstrual bleeding, prolonged menstrual bleeding, dysmenorrhea, and irregular menstruation); (3) alterations in hormone patterns including reduced estrogen excretion (REE), anovulation, abnormal luteal phase (ALP), and abnormal follicular phase (AFP) in women and abnormalities of LH, FSH, TSH, SHBG, inhibin-B and testosterone in men; (4) fecundability; and (5) pregnancy outcomes including spontaneous abortion, preterm delivery, low birth weight, and intrauterine growth retardation.

NCT ID: NCT00046137 Completed - Clinical trials for Osteoporosis, Postmenopausal

Combined Use of Teriparatide and Raloxifene in Postmenopausal Women With Osteoporosis

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare treatment with both teriparatide and raloxifene with teriparatide alone. The study will evaluate any side effects that may be associated with the two drugs and may help to determine whether teriparatide and raloxifene together can help patients with osteoporosis more than teriparatide alone.

NCT ID: NCT00046267 Completed - HIV Infections Clinical Trials

Niacin for Treatment of Elevated Cholesterol and Triglycerides in HIV-Infected Patients

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety, efficacy, and tolerability of extended-release niacin (Niaspan) in improving the level of fats in the blood of HIV-infected patients.

NCT ID: NCT00046306 Completed - Cancer Clinical Trials

Nevada Environmental Tobacco Smoke and Health Study

Start date: n/a
Phase: Phase 3
Study type: Interventional

Workplace exposure to secondhand cigarette smoke or environmental tobacco smoke (ETS)is widespread, effecting between 19 and 49% of the U.S. workforce. The first part of this study is designed to test whether exposure to ETS in the workplace effects a person's risk of developing chronic diseases such as cardiovascular disease and cancer. The second part of this study is designed to test whether antioxidant supplementation in this group of ETS exposed individuals can reduce their risk of developing chronic disease. The study will look at 375 non-smokers who either work on a casino floor or as bartenders or cocktail servers. Initial baseline data will be collected (questionnaires and blood samples taken) and the subjects will be randomized into one of three groups, placebo, low antioxidant supplementation and high antioxidant supplementation. They will be followed over a two-year period, coming in for follow-up testing every six months. Statistical analysis will be conducted to see whether this group of ETS exposed individuals has a greater risk of developing chronic disease and whether the use of antioxidant supplements can moderate any risks.

NCT ID: NCT00047983 Completed - Kidney Diseases Clinical Trials

Omega-3 Fatty Acids That Affect the Immune System in Kidney Transplant Patients

Start date: n/a
Phase: Phase 0
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of nutritional supplements in increasing the amount of omega-3 fatty acids (and arginine) in the red blood cell membranes and plasma of kidney transplant patients, and, secondarily, to compare patient compliance. The long-term goal of this study is to develop low risk therapies that will allow improved and lasting survival of donor tissue with minimal suppression of the immune system.

NCT ID: NCT00048282 Completed - HIV Infections Clinical Trials

HIV Prevention Preparedness Study

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

The purpose of this study is to provide researchers with information that will help them prepare for a future study to test the efficacy of two anti-HIV vaginal gels. This study will also estimate how likely people living in certain areas are to become infected with HIV and other infections passed during sex.