Clinical Trials Logo

Filter by:
NCT ID: NCT00197366 Terminated - HIV Infections Clinical Trials

Development of Resistance Mutations in Pregnant HIV-positive (+) Women Following Perinatal Antiretroviral Therapy in Israel

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

It has been shown that treatment of HIV-positive women with antiretroviral medication during pregnancy reduces the risk of HIV transmission to the child. However, such treatment could lead to the selection of resistant virus strains in the mother. The object of this study is to check HIV+ pregnant women for resistance mutations in HIV before and after the antiretroviral therapy they receive during pregnancy. HIV-positive newborns will also be tested, to see if a resistant virus strain was transmitted from mother to child.

NCT ID: NCT00196677 Terminated - Clinical trials for Glaucomatous Neuropathy

Study of Glaucoma Treatment With Food Additives

Start date: September 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if certain food additives are effective in the treatment of glaucoma, improving and reversing the progress of the disease.

NCT ID: NCT00160147 Terminated - Clinical trials for Psychosis and Behavioral Disturbances Associated With Dementia of the Alzheimer's Type

Treatment of Elderly Subjects With Psychosis and Behavioral Disturbances Associated With Dementia of the Alzheimer's Type

Start date: December 2005
Phase: Phase 3
Study type: Interventional

This is a 10-week study with bifeprunox and placebo in elderly subjects with psychosis and behavioral disturbances associated with dementia of the alzheimer's type.

NCT ID: NCT00152308 Terminated - Coronary Disease Clinical Trials

Non-Polymer-Based, Rapamycin-Eluting Stents to Prevent Restenosis

Start date: December 2004
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate the effectively of coating of coronary stents with two different doses of rapamycin for the prevention of coronary vessel re-blockage

NCT ID: NCT00151788 Terminated - Atherosclerosis Clinical Trials

Efficacy and Safety of the ACAT Inhibitor CS-505 (Pactimibe) for Reducing the Progression of Carotid Artery Disease. This Study is Also Known as CAPTIVATE.

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

The effects of pactimibe versus placebo on the progression of atherosclerosis in the carotid arteries will be assessed using standard ultrasound techniques.

NCT ID: NCT00147355 Terminated - HIV Infections Clinical Trials

Toxicity Substudy of Evaluation of Subcutaneous Proleukin in a Randomised International Trial (ESPRIT): TOXIL-2 Substudy

Start date: November 2005
Phase: Phase 3
Study type: Interventional

This substudy is an open-label, randomised study comparing the uptake of recombinant interleukin-2 (rIL-2) in HIV-1 infected individuals receiving different combinations of antiemetics and analgesic agents during rIL-2 dosing in ESPRIT. The design is a factorial one with 4 arms. All patients will receive regular ibuprofen and paracetamol from days 1-6 of the rIL-2 dosing cycle; in addition, patients will be randomised to receive one of two antiemetic combinations, i.e. ondansetron or metoclopramide with or without low dose codeine phosphate as an additional analgesic agent.

NCT ID: NCT00128791 Terminated - Clinical trials for Myocardial Infarction

Nitroprusside for Prevention of no-Reflow in Primary Angioplasty

Start date: January 2003
Phase: Phase 4
Study type: Interventional

In patients admitted with acute myocardial infarction, there is a total occlusion of a coronary artery. Even after emergency catheterization and angioplasty, in some patients, the resumed blood flow is suboptimal and impacts on heart function. The study is aimed at examining whether nitroprusside, an anti-hypertension medication, given directly into the coronary artery, can improve the blood flow after the removal of the obstruction that caused the infarction.

NCT ID: NCT00119184 Terminated - Breech Presentation Clinical Trials

Spinal Analgesia Versus No Analgesia: Study for External Cephalic Version

Start date: October 2002
Phase: Phase 1
Study type: Interventional

The purpose of this study is to examine whether spinal anesthesia affects the chances of successful external cephalic version (ECV) of a breech presenting fetus. Two study groups will be included; one will receive spinal anesthesia, the other will not. The non-spinal group will be permitted to cross over if ECV procedure is painful. The main outcome is success of ECV.

NCT ID: NCT00118573 Terminated - Clinical trials for Aortic Aneurysm, Abdominal

Comparison of Surveillance Versus Aortic Endografting for Small Aneurysm Repair

CAESAR
Start date: September 2004
Phase: Phase 4
Study type: Interventional

Objective of the present study is to compare endovascular repair versus surveillance and, eventually delay treatment in patients with small abdominal aortic aneurysms (AAA), with respect to patient survival, AAA rupture and AAA related death risks.

NCT ID: NCT00110721 Terminated - Colorectal Cancer Clinical Trials

GM-CT-01 Plus 5-Fluorouracil as Third- or Fourth-Line Therapy for Metastatic Colorectal Cancer

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

This is a Phase II, multi-center study of GM-CT-01 which has been shown to increase the anti-tumor activity of 5-fluorouracil (5-FU) in mice. 5-FU is a chemotherapy drug commonly used in cancer patients. In this Phase II study, patients with colon cancer which has spread, despite treatment with approved therapies, will receive GM-CT-01 plus 5-FU in monthly cycles for at least 2 cycles or until their disease progresses.