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Coquitlam, Canada Clinical Trials

A listing of Coquitlam, Canada clinical trials actively recruiting patients volunteers.

RESULTS

Found (87) clinical trials

The Effect of Low Dose Intra-operative Ketamine on Closed-loop Controlled General Anesthesia

For the primary outcome measure, the investigators hypothesize that controller performance with low-dose ketamine will be equivalent to the controller performance without low-dose ketamine. The primary outcome measure, controller performance, is the percentage of time during the maintenance phase when the depth-of-hypnosis (DOH) measure is within +-10 points of the ...

Phase

1.39 miles

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Family Healthy Living Early Intervention Program

The Childhood Healthy Weights Early Intervention Program (EIP) is a family-based pilot program that will promote healthy lifestyle practices for families whose children are off the healthy weight trajectory (e.g., BMI 85th percentile for age and sex) that do not need the intensive services of medically supervised programs. It is ...

Phase N/A

5.2 miles

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Regional Versus General Anesthesia for Promoting Independence After Hip Fracture

Hip fracture is a clinical condition that involves a break in the femur (hip bone) near where it attaches to the pelvis. Hip fractures occur more than 300,000 times each year in the US and over 1.6 million times each year worldwide. Over 90% of hip fractures occur in individuals ...

Phase N/A

5.83 miles

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Immediate Weight-Bearing Ankle Study

Ankle fractures are among the most common injuries, making up 9% of all fractures. Rotational ankle fractures are among the most common of all fractures, with an incidence averaging 4.2 per 1,000 individuals annually. These fractures range from minimal injuries amenable to non-surgical management to complex injuries with potential of ...

Phase N/A

5.83 miles

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Bowel Care and Cardiovascular Function After Spinal Cord Injury

The primary purpose of this study is to investigate the effects of topical anesthesia on cardiovascular changes triggered by bowel care in people with spinal cord injury. In people with spinal cord injury, episodes of high blood pressure are common during strong sensory stimuli such as those present during routine ...

Phase

5.94 miles

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Field Randomization of NA-1 Therapy in Early Responders

NA-1 is being developed as an emergency drug aimed at reducing global disability in patients with acute cerebral ischemia if administered early after symptom onset. The primary objective is to determine the efficacy of NA-1 in reducing global disability in patients with acute stroke. The secondary objectives are to determine ...

Phase

5.96 miles

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Healthy Lifestyles After Stroke

Participants recruited in this study will be randomly assigned to either the Healthy Lifestyle Training Program, or Attention Control Memory Training Program. Individuals in the Healthy Lifestyle Training Program will each receive 7 lifestyle coaching telephone-sessions (30-60 minutes) with a trained lifestyle coach over a 6 month period. Individuals in ...

Phase N/A

5.96 miles

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Occupational Recovery After First Episode Psychosis

This primary objective of this project is to assess, in early psychosis clients, the IPS vocational support model that is the "gold standard" for patients with chronic illness. Specifically, the investigators aim to maximize the chances of employment after recovery from the first acute episode, and provide work experience that ...

Phase N/A

5.96 miles

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The NEUROlogically-impaired Extubation Timing Trial

Thousands of patients suffer severe brain injuries every year, from causes such as trauma, stroke, and infection. Extensive clinical research in weaning from mechanical ventilation has led to recommendations for prompt extubation following a successful trial of spontaneous breathing in general intensive care unit (ICU). However, little evidence exists to ...

Phase N/A

5.96 miles

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National Observational Study of Clinical Practices in Deceased Organ Donation

This prospective cohort study enrols consecutive adult deceased organ donors with a waiver of research consent and collects various data related to deceased donor care in the ICU from the time of consent for donation to the time of organ recovery. Clinical data includes donor characteristics, type of donation (after ...

Phase N/A

5.96 miles

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