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NCT ID: NCT01612091 Withdrawn - Critical Care Clinical Trials

The Monitoring Messenger: Mobile Patient Monitoring for the Pediatric Intensive Care Unit

Start date: November 2013
Phase: N/A
Study type: Interventional

The Mobile Messenger is a unified, portable and intelligent device that integrates information from multiple patient monitors, mechanical ventilators, infusion pumps and clinical information systems on a mobile platform. It will allow nurses, respiratory therapists and physicians to continuously monitor and coordinate care of critically ill patients. This study will use a participatory design process to guide the design of an integrated mobile device. Next, we will evaluate the proposed device in a simulated ICU setting.

NCT ID: NCT01609439 Withdrawn - Hypocalcemia Clinical Trials

Preoperative Vitamin D for Post-thyroidectomy Hypocalcemia

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

The purpose of this study is to determine if pre-operative vitamin D supplementation lowers the incidence of post-operative transient or permanent hypoparathyroidism in patients undergoing total thyroidectomy.

NCT ID: NCT01607671 Withdrawn - Clinical trials for Ischemic Optic Neuropathy

Treatment Study for Ischemic Optic Neuropathy With Opthalmic Timolol Maleate 0.5%

Start date: June 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the feasibility of rapid evaluation and administration of ophthalmic Timolol maleate in the treatment of non-arteritic anterior ischemic optic neuropathy. Secondary goals are to evaluate if such treatment reduces the progression or improves recovery of patients who are randomly assigned to treatment versus standard of care.

NCT ID: NCT01604200 Withdrawn - Clinical trials for Focus of Study is on Dentist's Attitudes Toward BP Measures

Dental PROBE (Dental Practice suRvey of Office Blood Pressure mEasurement)

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

20% of Canadians are hypertensive with approximately 200,000 new cases each year. Early detection of hypertension affects outcomes, reducing the risk for heart attack, stroke, kidney disease, and dementia. Screening strategies are required to identify the more than one third of Canadians with unrolled high blood pressure, in particular, younger men unaware of their condition, women over sixty years old, and underserved groups. A collaborative practice model linking dentists to other healthcare providers in a reporting network is a promising model for hypertension detection and management. There are 20,129 licensed dentists in Canada who graduate with the ability to measure blood pressure, and 74% of the population visits a dentist each year. This represents an opportunity, but information is required on Dental attitudes toward screening for hypertension before attempting to initiate a screening model. To engage dentists in hypertension detection requires an understanding of the practice environment and the factors that shape their beliefs, attitudes and behaviours regarding routine hypertension screening in their practices.

NCT ID: NCT01602991 Withdrawn - Obesity Clinical Trials

Clinic-based Nasopharyngoesophagogastroscopy Following Bariatric Surgery

EGScan
Start date: May 2012
Phase: N/A
Study type: Interventional

This study aims to determine that this new technology, nasopharyngoendoscopy, is just as effective in diagnosing problems as the current gold standard.

NCT ID: NCT01602432 Withdrawn - Cancer Clinical Trials

Implementing a Tool to Identify Risk for Venous Thromboembolism in Cancer Patients

Start date: November 2012
Phase:
Study type: Observational

Cancer increases the risk of deep vein blood clots and clots traveling to the lungs (emboli) which cause morbidity (leg swelling, pain, and shortness of breath), sudden death, delays cancer treatment, and decreases cancer survival by 66% compared to similar cancer patients without blood clots. Blood thinners may prevent clots but major bleeding is also a problem, so preventive therapies are not used routinely. Identifying patients at highest risk for clots is critical. A tool exists but it has not been used outside of research. We propose to study how to apply this tool in clinical practice and test if it works.

NCT ID: NCT01599429 Withdrawn - Clinical trials for Acute Myeloid Leukemia

Study of the Predictive Marker FLT in Patients Suffering From AML

TEP-FLT-LMA
Start date: October 31, 2011
Phase:
Study type: Observational

Positron emission tomography uses various radioactive tracers to measure the metabolic activity in a none-invasive way, and specially to follow the activity of the disease during the treatments. Among those new tracers, fluorothymidine (18F-FLT) arouses a lot of interest. This new tool would allow to image and follow time wise acute myeloid leukemia (AML). The investigators want, with the (18F-FLT), to characterise the aggressivity of the tumors and the prognostic before and after chemotherapy treatment. The aim of this study is to be able to identify earlier the responders, because if they are detected sooner, these patients will benefit from more aggressive treatments.

NCT ID: NCT01591980 Withdrawn - Headache Clinical Trials

Effects of Perioperative Pregabalin for Post-Craniotomy Pain

Start date: August 2013
Phase: Phase 4
Study type: Interventional

Objective: To compare the incidence of chronic pain at 3 months among adults undergoing craniotomy between those received two different doses of pregabalin and those receiving placebo.

NCT ID: NCT01549496 Withdrawn - Hypertension Clinical Trials

A Drug Interaction Study of Boceprevir in Combination With Amlodipine or Diltiazem in Healthy Volunteers

Start date: May 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the pharmacokinetic interactions between the hepatitis C NS3 protease inhibitor boceprevir and the calcium channel blockers amlodipine and diltiazem in healthy volunteers.

NCT ID: NCT01542216 Withdrawn - Breast Cancer Clinical Trials

Evaluation of Nutrition and Metabolism in Breast Cancer Patients

Start date: February 2012
Phase: N/A
Study type: Interventional

With the increased success in breast cancer therapies, survivors develop unhealthy changes in body composition, such as muscle loss and fat gains, which lead to increased risk of cardiovascular disease and diabetes in survivorship. This study will examine the effects of a nutrition, cardiovascular and strength exercise program compared with a yoga program (representing usual care) on body composition and metabolism in recently diagnosed breast cancer patients. Nutrition and exercise may improve various body composition and metabolic parameters, which may improve quality of life in survivorship, reduce risk of recurrence and reduce the risk of developing cardiovascular disease and diabetes in survivorship.