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NCT ID: NCT00808535 Not yet recruiting - Diabetes Clinical Trials

Cardiac Magnetic Resonance Imaging for Detecting Endothelial Dysfunction

Start date: February 2009
Phase: N/A
Study type: Observational

The goal of this research study is to demonstrate that Cardiac Perfusion MRI with Vasomotor Stress may serve as a non-invasive and less risky imaging technique for detecting non-obstructive perfusion deficits and/or abnormalities in myocardial blood flow (MBF) in patients with endothelial dysfunction. This is a controlled study, which will enroll approximately 60 subjects (30 diabetics and 30 non-diabetics to serve as healthy controls), and will include male and non-pregnant females, between the ages 18-50 years. All eligible participants will sign an informed consent and will complete a Lifestyle Questionnaire. They will undergo blood work which includes: - 2-hour Oral Glucose Tolerance Test and Fasting Labs for Glucose, Insulin, C-Peptide, HbA1c, Creatinine, and Lipid Panel. - Urine Albumin to Creatinine ratio for microalbuminuria. - Serum inflammatory markers: E-selectin, homocysteine, ADMA, VCAM, IL-6, TNFalpha, hs-CRP and PAI-1. After blood work, all participants will undergo cardiac MR perfusion imaging procedure with Cold Pressor Test and Adenosine Stress Test.

NCT ID: NCT00773864 Not yet recruiting - Clinical trials for Methicillin-Resistant Staphylococcus Aureus

Mastering Hospital Antimicrobial Resistance and Its Spread Into the Community-Healthcare Workers

MOSAR
Start date: October 2008
Phase: N/A
Study type: Observational

Medical staff will be screened for MRSA and ESBL (including: doctors, nurses, nurse aids, physical therapists, dietitians, Janitors and other medical staff). PURPOSE: To define the carriage of, and risk factors for carriage of resistant organisms among healthcare employees of carriers of resistant bacteria. To define activities of healthcare employees who likely to lead to dissemination of resistant bacteria in rehabilitation centers.

NCT ID: NCT00773799 Not yet recruiting - Clinical trials for Methicillin-Resistant Staphylococcus Aureus

Mastering Hospital Antimicrobial Resistance and Its Spread Into the Community

MOSAR
Start date: October 2008
Phase: N/A
Study type: Observational

Data on occurrence of antimicrobial resistant bacteria acquisition in rehabilitation centers will be collected. After removal of patient identifiers, information regarding the patients population will be entered into electronic sheet. The phase will last twelve months in each center.

NCT ID: NCT00763828 Not yet recruiting - Clinical trials for ST-Elevation Myocardial Infarction

Can Hypothermia be Incorporated Into Primary Angioplasty for Heart Attack?

CHIPAHA
Start date: January 28, 2024
Phase: N/A
Study type: Interventional

The hypothesis of this study is that consciously sedated patients suffering from ST-elevation myocardial infarction can be rapidly and safely cooled to a state of therapeutic hypothermia (32 to 34 degrees C) using the LRS ThermoSuit System prior to percutaneous coronary intervention.

NCT ID: NCT00758849 Not yet recruiting - Parkinson's Disease Clinical Trials

Fipamezole in Neurogenic Orthostatic Hypotension

Foehn
Start date: September 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Fipamezole is effective in the treatment of orthostatic hypotension and related symptoms in multiple system atrophy and Parkinson's disease.

NCT ID: NCT00752882 Not yet recruiting - Clinical trials for Pseudomonas Aeruginosa Meningitis

Ceftazidime Pharmacokinetic in Cerebrospinal Fluid Between Continuous and Intermittent Administration

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

Meningitis is an infection where morbidity and mortality depend on the delay of the initial treatment for a good prognostic. The antibiotherapy rapidity allows to decrease the mortality. Intermittent administration of ceftazidime is a reference treatment of Pseudomonas aeruginosa meningitis. In the case of Pseudomonas aeruginosa pneumopathy, ceftazidime can be administered by intermittent injections or by continuous perfusion. The continuous administration of ceftazidime is not validated in Pseudomonas aeruginosa meningitis. However, ceftazidime is a time dependant antibiotic and continuous treatment would provide a more efficient therapeutic. The aim of this study is to determine if the continuous administration of ceftazidime could permit a better therapeutic practice of Pseudomonas aeruginosa meningitis compared with intermittent administrations.

NCT ID: NCT00752024 Not yet recruiting - Clinical trials for Hypertensive Intracerebral Hemorrhage

Stereotactic Aspiration and Thrombolysis of Intracerebral Hemorrhage: a Prospective Controlled Study

SATIH
Start date: September 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the superiority of effect of the modified micro-invasive aspiration and drainage and conservative medical therapy in the treatment of ICH spontaneously hypertensive scientifically.

NCT ID: NCT00751374 Not yet recruiting - Clinical trials for Rate of Exit Site Infection

Topical Gentamicin Cream Versus Alternating Gentamicin and Mupirocin Cream in Peritoneal Dialysis

Start date: September 2008
Phase: Phase 4
Study type: Interventional

Catheter-related infection, namely exit site infection and peritonitis, is the commonest complication of peritoneal dialysis. This complication causes significant morbidity and mortality in patients requiring peritoneal dialysis. Topical application of mupirocin 2% cream was first proven to be effective in reduction of staphylococcus-related catheter infection in 1990s. Subsequent randomized trial published in 2005 showed that gentamicin cream was superior to mupirocin 2% cream in reducing both Gram's positive and Gram's negative related catheter infection. However, a retrospective report published in 2007 puts the use of prophylactic antibiotic cream into a question. It reported an emergency of non-tuberculous mycobacterial infection in a dialysis center in Hong Kong after practising prophylactic application of gentamicin cream at the catheter exit site. The following prospective, randomized and open-label study aims to find out an optimal regimen of topical antibiotic prophylaxis in patients requiring peritoneal dialysis.

NCT ID: NCT00720967 Not yet recruiting - Clinical trials for Cardiovascular Disease

Preop Hemodialysis or Intraop Ultrafiltration for Patients With Severe Renal Dysfunction Undergoing Open Heart Surgery

SeRenaD-CPB
Start date: November 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether preoperative hemodialysis or intraoperative modified ultrafiltration are effective for patients with non-dialysis dependent severe renal dysfunction undergoing open heart surgery.

NCT ID: NCT00662181 Not yet recruiting - HIV Infections Clinical Trials

Follow-up on the HIGH: Low Study - the Longterm Effects of Growth Hormone

Start date: May 2008
Phase: N/A
Study type: Observational

A follow-up study on the randomized, controlled, double-blind HIGH: low study. We will examine the participants from the HIGH: low study min. 6 months after finishing the HIGH: low study. We will look at the parameters: quality of life, sugar-metabolism, fat-metabolism, fat-redistribution and cytokines. The study will use the participants control visit, and the only additional examination will be the danish MOS-HIV questionnaire.