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NCT ID: NCT01188187 Completed - Prostate Cancer Clinical Trials

Comparison of Docetaxel/Prednisone to Docetaxel/Prednisone in Combination With OGX-011 in Men With Prostate Cancer

SYNERGY
Start date: November 2010
Phase: Phase 3
Study type: Interventional

This Phase 3 study has been designed to confirm that adding custirsen to standard first-line docetaxel/prednisone treatment can slow tumor progression and enhance survival outcomes compared to standard first-line docetaxel/prednisone treatment alone. This will be a randomized, open-label, multicenter, international trial. Treatment will consist of docetaxel/prednisone/custirsen vs. docetaxel/prednisone. A total of at least 1000 patients will be randomized. Patients will be randomly assigned with equal probability to the two arms.

NCT ID: NCT01187589 Completed - COPD Clinical Trials

PulseHaler Drug Deposition Study in Chronic Obstructive Pulmonary Disease Patients

Start date: December 2010
Phase: N/A
Study type: Interventional

This study is aimed at finding the effect of PulseHalerâ„¢ with Albuterol on Lung Deposition of Aerosol and on Pulmonary Functions in COPD Patients

NCT ID: NCT01185899 Completed - Clinical trials for Acute Coronary Syndrome

Usefulness of High-frequency QRS Analysis in the Evaluation of Patients With Chest Pain

Start date: August 2010
Phase: N/A
Study type: Observational

Accurate detection of a heart attack (an acute myocardial infarction) is one of the most pressing needs in medicine. Recordings of the electrocardiogram (ECG) (electrical activity of the heart) are one of the first tools used to diagnose a heart attack, but the ECG is not very accurate, especially at the beginning of a heart attack. A new technique for analysing a special part of the ECG may provide more accurate detection of a heart attack. The study hypothesis is that this new technique, the HFQRS analysis, will provide important additional information to that available from the regular ECG.

NCT ID: NCT01185327 Completed - Rumination Clinical Trials

Do Isreali Infants of Ethiopian Origin Mother Regurgitate More Than Other Infants?

Start date: August 2010
Phase: N/A
Study type: Observational

Nursing team of well baby nursery at Hillel Yaffe medical center in Hadera, Israel have noticed that infant of Ethiopian-origin mothers regurgitate more than other infants. Probably, these infants are breastfeed much more than other infants. Some Ethiopian-origin mothers are used to eat teff-flower porridge during the last weeks of pregnancy and after birth, in order to expand milk production. Study goal is to find out if infants of Ethiopian-origin mother do regurgitate more than others, and if they weight gain is similar to other infants. Another goal is to find out if breastfeeding mothers of Ethiopian origin do eat that porridge, and if there is any difference between those who do eat that porridge and those who do not.

NCT ID: NCT01183780 Completed - Colorectal Cancer Clinical Trials

A Study in Second Line Metastatic Colorectal Cancer

Start date: December 2, 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare overall survival in participants with metastatic colorectal cancer treated with either ramucirumab and FOLFIRI or placebo and FOLFIRI.

NCT ID: NCT01183000 Completed - Cesarean Section Clinical Trials

Closure of Peritoneum at Cesarean Section and Postoperative Adhesion

cs adhesions
Start date: January 16, 2010
Phase: N/A
Study type: Interventional

Objective: To determine the effect of non-closure of the visceral and parietal peritoneum during Cesarean section on the formation of adhesions. Study design: A prospective randomized trial of 533 women undergoing primary Cesarean section; 256 were randomized to non closure and 277 to closure of the peritoneum. At a subsequent cesarean,he presence of adhesions and their severity was evaluated at several sites: between the layers of the abdominal wall, between the bladder and the abdominal wall, between bladder and uterus, between the uterus and the abdominal wall, and between the bowels and the pelvic organs. A cumulative adhesion score was calculated.

NCT ID: NCT01182974 Suspended - Sepsis Clinical Trials

Paracetamol Toxicity in Septic Patients

Start date: August 2010
Phase: Phase 3
Study type: Interventional

The investigators will examine the toxicity of therapeutic doses of paracetamol in patients in severe sepsis. Patients with fever and severe sepsis will be randomized to receive paracetamol or dypirone. The investigators will monitor blood glutathione and liver enzymes to look for potential toxicity.

NCT ID: NCT01182961 Not yet recruiting - Elderly Clinical Trials

The Use of Virtual Reality for the Gait Training of Elderly Fallers

VR-Fallers
Start date: September 2010
Phase: N/A
Study type: Interventional

The study aims to investigate the efficacy of gait training using virtual reality to decrease the risk of falls in elderly idiopathic fallers. The investigator hypothesize that training with virtual reality would increase the ability to perform in the "real world" environment and decrease the risk of falls in elderly adults.

NCT ID: NCT01182493 Completed - Clinical trials for Diabetes Mellitus, Type 2

OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump Therapy

OpT2mise
Start date: December 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the comparative effectiveness of insulin pump therapy versus multiple daily injections in insulin-taking type 2 Diabetes Mellitus who are sub optimally controlled with multiple daily injections (MDI).

NCT ID: NCT01181466 Completed - COPD Clinical Trials

AeriSeal® System for Lung Volume Reduction in Patients With Advanced Emphysema

Start date: August 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to assess the procedural and post-procedural safety and efficacy of AeriSeal therapy at up to 4 subsegments during a single treatment session in patients with GOLD Stage III/IV homogeneous or heterogeneous emphysema.