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Ottawa Hospital Research Institute

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OTTAWA, Ontario K1H 8L6
Global Leader in Cancer
Global Leader in Lung Cancer
Conducts research for Non-Small Cell Lung Cancer
Conducts research for Breast Cancer
Conducts research for Colorectal Cancer
219 reported clinical trials
26 medical researchers
Photo of Ottawa Hospital Research Institute in OTTAWAPhoto of Ottawa Hospital Research Institute in OTTAWAPhoto of Ottawa Hospital Research Institute in OTTAWA

Summary

Ottawa Hospital Research Institute is a medical facility located in OTTAWA, Ontario. This center is recognized for care of Cancer, Lung Cancer, Non-Small Cell Lung Cancer, Breast Cancer, Colorectal Cancer and other specialties. Ottawa Hospital Research Institute is involved with conducting 219 clinical trials across 274 conditions. There are 26 research doctors associated with this hospital, such as John Hilton, MD, Dar Dowlatshahi, MD, Scott A Laurie, and Scott C. Morgan.

Area of expertise

1Cancer
Global Leader
Ottawa Hospital Research Institute has run 16 trials for Cancer. Some of their research focus areas include:
TP53 positive
Stage IV
HER2 positive
2Lung Cancer
Global Leader
Ottawa Hospital Research Institute has run 15 trials for Lung Cancer. Some of their research focus areas include:
Stage IV
Stage III
PD-L1 positive

Top PIs

Clinical Trials running at Ottawa Hospital Research Institute

Bleeding
Prostate Cancer
Melanoma
Non-Small Cell Lung Cancer
Multiple Myeloma
Lymphoma
Skin Cancer
Plasma Cell Neoplasms
Stroke
Cancer
Image of trial facility.

Lower INR Warfarin

for Mechanical Valve Patients

This study evaluates the use of a lower INR target (1.5 to 2.5) in patients with a mechanical bileaflet heart valve in the aortic position. This study will inform physicians about whether a lower INR target will decrease the risk of bleeding or increase the risk of blood clot formation and stroke. These results have the potential to reduce the burden of bleeding in patients with a mechanical heart valve who require lifelong warfarin (Coumadin) treatment.
Recruiting2 awards Phase 33 criteria
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Aggressive Blood Pressure Management

for Brain Hemorrhage

The vast majority of intracerebral hemorrhage (ICH) patients present with elevated blood pressure(BP). Management of BP is controversial with two competing rationales. There is some evidence that hyperacute treatment may improve outcomes by reducing the rate of hematoma expansion. Physicians have been reluctant to reduce BP early after ICH onset, fearing reduced cerebral blood flow (CBF) will increase ischemia and increase the risk of further damage. Other confounding mediators to further ischemic injury following ICH include increased platelet activity, withdrawal of antithrombotic therapy, endothelial dysfunction, inflammation and hypercoagulability. This study is phase II of the ICH-ADAPT study. The investigators hypothesize that aggressive antihypertensive therapy will alter the natural history of heamatoma growth, improving outcomes after Intracranial Hemorrhage (ICH). The previous phase I ICH-ADAPT study has established the safety of early BP treatment. The investigators have designed a phase II study in which ICH patients are randomized to aggressive versus conservative BP treatment using a deferred consent procedure. An adaptive randomization will be used to treat BP to \< 140 mmHg SBP or \< 180 mmHg SBP. Treatment must be implemented as soon as possible after radiological confirmation of diagnosis. Antihypertensive therapy must begin within 6 hours of symptom onset. The patient will be re-imaged 24 hours later. The patient will have continuous non-invasive BP and heart rate(HR) monitoring for a minimum of 24 hours. Antihypertensive drug use and dosage will be recorded with BP and HR. Patients will be monitored regularly until study completion. MRI's will be done at 48 hours, day 7 and day 30. This imaging will help to detect ischemic changes that may occur. Blood will be collected at the same time as the MRI. Blood analysis will be done to possibly identify biomarkers that may be putative mediators of ischemic injury in ICH patients.
Recruiting1 award Phase 24 criteria
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rFVIIa

for Hemorrhagic Stroke

The objective of the rFVIIa for Acute Hemorrhagic Stroke Administered at Earliest Time (FASTEST) Trial is to establish the first treatment for acute spontaneous intracerebral hemorrhage (ICH) within a time window and subgroup of patients that is most likely to benefit. The central hypothesis is that rFVIIa, administered within 120 minutes from stroke onset with an identified subgroup of patients most likely to benefit, will improve outcomes at 180 days as measured by the Modified Rankin Score (mRS) and decrease ongoing bleeding as compared to standard therapy.
Recruiting1 award Phase 34 criteria

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Frequently asked questions

What kind of research happens at Ottawa Hospital Research Institute?
Ottawa Hospital Research Institute is a medical facility located in OTTAWA, Ontario. This center is recognized for care of Cancer, Lung Cancer, Non-Small Cell Lung Cancer, Breast Cancer, Colorectal Cancer and other specialties. Ottawa Hospital Research Institute is involved with conducting 219 clinical trials across 274 conditions. There are 26 research doctors associated with this hospital, such as John Hilton, MD, Dar Dowlatshahi, MD, Scott A Laurie, and Scott C. Morgan.