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Résultats de recherche

By obtaining clinical specimens from participants with triple negative breast cancer (TNBC), colorectal cancer (CRC), high grade serous ovarian cancer (HGSOC), and other select tumor types to establish and profile as freshly implanted tumors in mice, the aim of this study is to identify agents with predicted activity in the host patient while also potentially providing them with personalized cancer treatment options

Conditions:
Colorectal Neoplasms | Colorectal Cancer | Breast Cancer | Breast Neoplasms | Ovarian Cancer | Ovarian Neoplasm
Emplacement:
  • Princess Margaret Cancer Centre, Toronto, Ontario, Canada
Sexe:
ALL
Âges:
Over 18

The proposed project mainly aims to investigate the microbial processes leading to dietary metabolites production, independently of long-term microbiota adaptation to the diet, by measuring the microbiota-derived metabolite production from a meal sequence rich in saturated fatty acids (SFA) or the same meals but rich in polyunsaturated fatty acids (PUFA) in individuals with or without obesity and Type 2 diabetes (T2D)

Conditions:
Obesity, Abdominal | Diabete Type 2
Emplacement:
  • Institut sur la nutrition et les aliments fonctionnels - INAF, Québec, Quebec, Canada
Sexe:
ALL
Âges:
45 - 65

This clinical trial is studying the safety and potential anti-tumor activity of an investigational drug called ARV-393 in patients diagnosed with advanced Relapsed/Refractory non-Hodgkin's lymphoma to determine if ARV-393 may be a possible treatment option. ARV-393 is thought to work by breaking down a protein present in many types of non-Hodgkins lymphomas, which may prevent, slow or stop tumor growth. This is the first time ARV-393 will be used by people. The investigational drug will be given as an oral tablet.

Conditions:
Relapsed/Refractory (R/R) Angioimmunoblastic T-cell Lymphoma...
Emplacement:
  • Clinical Trial Site, Toronto, Ontario, Canada
  • Clinical Trial Site, Montreal, Quebec, Canada
Sexe:
ALL
Âges:
Over 18

The objective is to observe the evolution of walking parameters during the surgery process and find which of all calculated walking parameters represent the best indicators of functional disabilities and postoperative recovery for patient with lumbar spinal stenosis.

Conditions:
Lumbar Spinal Stenosis
Emplacement:
  • Université du Québec à Trois-Rivières, Trois-Rivieres, Quebec, Canada
Sexe:
ALL
Âges:
Over 18

The purpose of this study is to find out what effects of using adaptive radiotherapy to deliver chest radiation has on the ability to control lung cancer and side effects.

Conditions:
Small Cell Lung Cancer
Emplacement:
  • Cross Cancer Institute, Edmonton, Alberta, Canada
Sexe:
ALL
Âges:
Over 18

Tree nut immunotherapy Route Assessment and DEvelopment (TRADE) is a randomized controlled trial that evaluates the efficacy and safety of sublingual immunotherapy and lower, more tolerable, doses of oral immunotherapy than currently in use.

Conditions:
Food Allergy | Tree Nut Allergy
Emplacement:
  • McMaster University Medical Centre, Hamilton, Ontario, Canada
Sexe:
ALL
Âges:
1 - 16

This phase III trial studies magnetic resonance imaging (MRI) surveillance and prophylactic cranial irradiation (PCI) to see how well they work compared to MRI surveillance alone in treating patients with small cell lung cancer. MRI scans are used to monitor the possible spread of the cancer with an MRI machine over time. PCI is radiation therapy that is delivered to the brain in hopes of preventing spread of cancer into the brain. The use of brain MRI alone may reduce side effects of receiving PCI and prolong patients' lifespan. Monitoring with MRI scans alone (delaying radiation until the actual spread of the cancer) may be at least as good as the combination of PCI with MRI scans.

Conditions:
Extensive Stage Lung Small Cell Carcinoma | Limited Stage Lung Small Cell Carcinoma | Lung Small Cell Carcinoma
Emplacement:
  • BCCA-Vancouver Island Cancer Centre, Victoria, British Columbia, Canada
  • Juravinski Cancer Centre at Hamilton Health Sciences, Hamilton, Ontario, Canada
  • The Research Institute of the McGill University Health Centre (MUHC), Montreal, Quebec, Canada
  • Doctor H. Bliss Murphy Cancer Centre, St. John's, Newfoundland and Labrador, Canada
  • University Health Network-Princess Margaret Hospital, Toronto, Ontario, Canada
  • Allan Blair Cancer Centre, Regina, Saskatchewan, Canada
  • CancerCare Manitoba, Winnipeg, Manitoba, Canada
  • Lakeridge Health Oshawa, Oshawa, Ontario, Canada
  • CHU de Quebec-L'Hotel-Dieu de Quebec (HDQ), Quebec City, Quebec, Canada
  • Atlantic Health Sciences Corporation-Saint John Regional Hospital, Saint John, New Brunswick, Canada
  • Odette Cancer Centre- Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
  • Centre Hospitalier Regional de Trois-Rivieres, Trois-Rivieres, Quebec, Canada
Sexe:
ALL
Âges:
Over 18

The purpose of the present study is to follow unpaid caregivers of ABI survivors in Nova Scotia over time to learn more about their experiences. The study is funded by the Government of Nova Scotia (i.e. Department of Health and Wellness). The present longitudinal cohort study will help increase knowledge about ABI caregivers at a provincial level. Findings will also be used in developing future interventions to help caregivers in this population. The goals of the research study are: 1. To understand the natural experiences of unpaid caregivers over time. More specifically, the investigators hope to learn about the experiences of unpaid caregivers of acquired brain injury survivors in Nova Scotia. 2. To examine the connection between study demographic variables (e.g. the amount of time spent caregiving in hours per week), and psychological outcome variables (e.g. caregiver burden). 3. To learn about the relationship between psychological outcome variables (e.g. psychological distress and savouring). 4. To provide a platform for future studies using the Trials within Cohort (TwiC) study design.

Conditions:
Caregivers
Emplacement:
  • IWK Health Centre, Halifax, Nova Scotia, Canada
Sexe:
ALL
Âges:
Over 18

The liver produces a protein called alpha-1 antitrypsin (AAT). AAT is normally released into the bloodstream. In some people, the liver makes an abnormal version of the AAT protein, called Z-AAT. Making an abnormal version of the AAT protein can result in liver disease as Z-AAT builds up in liver cells, which leads to liver problems such as liver scarring (fibrosis), continuing liver damage (cirrhosis), and eventually endstage liver disease. Fazirsiran is a medicine that reduces the creation of the Z-AAT protein and thus the build-up of this abnormal protein in the liver. People with this type of liver disease who already have mild liver scarring will take part in the study. They will be treated with fazirsiran or a placebo for about 2 years. This study will check the long-term safety of fazirsiran, whether participants tolerate the treatment and if there are any effects on liver scarring. A liver biopsy, a way of collecting a small tissue sample from the liver, will be taken twice during the study.

Conditions:
Alpha1-Antitrypsin Deficiency
Emplacement:
  • Inspiration Research Limited, Toronto, Ontario, Canada
Sexe:
ALL
Âges:
18 - 75

Schizophrenia and depression are among the most disabling disorders in all of medicine. Cognitive deficits play a key role in patients' disability, affecting their capacity to contribute actively to society by sustaining employment or academic activity. Moreover, cognitive difficulties tend to persist even after the stabilization of other clinical symptoms. Verbal memory and emotion regulation are two important cognitive domains that are impaired in schizophrenia and depression and are associated with patients' functional outcomes. In this study, we are using brain imaging to investigate the brain mechanisms underlying these cognitive deficits in these populations.

Conditions:
Schizophrenia / Schizoaffective Disorder | Depression / Major Depressive Disorder
Emplacement:
  • Royal Ottawa Mental Health Center, Ottawa, Ontario, Canada
Sexe:
ALL
Âges:
18 - 65