AzTrials
AzTrials

Research institution

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's Clinical Trials

Studies where London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's is the lead sponsor: what is enrolling now, by phase, condition and country.

707 registered studies

In numbers

Open to volunteers
98
Active
136
With results posted
14
All registered
707

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 98
  • Limited Stage Small-Cell Lung Cancer

    A Randomized Trial of Standard vs. Hypofractionated Accelerated Radiotherapy for Progression in Limited-Stage Small Cell Lung Cancer

    • Not yet recruiting
    • Age: 18 years and older
    • Phase 2/3
    • Surgery or procedure

    This study aims to determine whether an abbreviated course of thoracic radiotherapy, delivered in five fractions over one week between chemotherapy cycles, improves progression-free survival compared with standard radiotherapy…

    Trial name
    SHARP SCLC (NCT07920549)
    Testing
    Radiation Therapy, Hypofractionated Radiation Therapy, Chemotherapy
    Where
    Canada
    Volunteers
    150 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
    Can I take part? SHARP SCLC
  • Idiopathic Subglottic Stenosis, Subglottic Stenosis (SGS)

    Pirfenidone for Idiopathic Subglottic Stenosis: A Pilot Trial of Tolerability and Feasibility

    • Not yet recruiting
    • Age: 18 to 65 years
    • Phase 1

    Idiopathic subglottic stenosis (iSGS) is a rare condition where scar tissue forms just below the vocal cords and in the upper windpipe, making the airway narrow.

    Trial name
    NCT07654517
    Testing
    Pirfenidone
    Where
    2 sites in Canada
    Volunteers
    44 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
  • PTSD, Post-traumatic Stress Disorder

    Deep Brain Reorienting in Post-traumatic Stress Disorder

    • Recruiting
    • Age: 18 to 65 years
    • Lifestyle or therapy programme

    This study will evaluate the efficacy of a therapeutic treatment, Deep Brain Reorienting (DBR), for PTSD (Post-traumatic Stress Disorder). Participants will be randomized to either the DBR treatment, or wait-list condition.

    Trial name
    NCT04317820
    Testing
    Deep Brain Reorienting (DBR)
    Where
    Canada
    Volunteers
    234 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
  • Alzheimer's Disease (AD), Cognitive Impairment

    BioMIND Biospecimen Repository

    • Enrolling by invitation
    • Age: 18 years and older
    • Observational study

    The purpose of the BBR is to facilitate scientific research by serving as a local and external resource for the distribution of human blood and CSF biospecimens, together with their corresponding clinical data, to internal and…

    Trial name
    BBR (NCT07912736)
    Testing
    blood sample and optional csf collection
    Where
    Canada
    Volunteers
    1,000 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
    Can I take part? BBR
  • Depression - Major Depressive Disorder, Generalized Anxiety Disorder (GAD)

    Microbiota Modulation for Psychiatry Patients

    • Not yet recruiting
    • Age: 16 to 45 years
    • Phase 1

    The investigators aim to confirm pilot study findings (REB 119638) on the effects of delayed release apple cider vinegar (drACV).

    Conditions
    Depression - Major Depressive Disorder, Generalized Anxiety Disorder (GAD), Anxiety
    Trial name
    ACV-MTPIES-002 (NCT07899424)
    Testing
    Dietary Supplement: Acetate (Apple Cider Vinegar)
    Volunteers
    62 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
  • Dementia, Agitation

    Virtual Reality to Advance Dementia Care and Quality of Life

    • Not yet recruiting
    • Age: 55 years and older
    • Lifestyle or therapy programme

    The goal of this feasibility clinical trial is to learn whether supervised virtual reality (VR) sessions can be safely and practically provided to adults aged 55 years and older with moderate-to-severe dementia who experience…

    Conditions
    Dementia, Agitation, Behavioural and Psychological Symptoms of Dementia, Major Neurocognitive Disorder
    Trial name
    VR-Care (NCT07893678)
    Testing
    Supervised Virtual Reality Sessions
    Where
    2 sites in Canada
    Volunteers
    10 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
    Can I take part? VR-Care
  • Symptom Tracking, Cardiology

    AI-CLINIC: A Prospective Multisite Feasibility and Safety Study of AI-Assisted Pre-Consultation History-Taking in Outpatient Cardiology

    • Not yet recruiting
    • Age: 18 years and older
    • Observational study

    An accurate medical diagnosis depends on the doctor getting a complete picture of the patient's health story, but clinic visits are short.

    Conditions
    Symptom Tracking, Cardiology, Medical History Taking
    Trial name
    AI-CLINIC (NCT07883304)
    Testing
    AI Interview
    Volunteers
    60 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
    Can I take part? AI-CLINIC
  • Juvenile Idiopathic Arthritis, Children

    M3-JIA: Making Mindfulness Matter for Children With JIA

    • Recruiting
    • Age: 4 to 12 years
    • Lifestyle or therapy programme

    The investigator will evaluate the efficacy of M3©, an intervention for patients with JIA and their caregivers. Children with Juvenile arthritis and their parents will attend an 8 week online program called Making Mindfulness…

    Conditions
    Juvenile Idiopathic Arthritis, Children, Mental Health, Mental Well-being
    Trial name
    M3-JIA (NCT06376149)
    Testing
    M3 Intervention group, M3 Waitlist Group
    Where
    3 sites in Canada
    Volunteers
    74 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
    Can I take part? M3-JIA
  • Total Hip Arthroplasty, Computer-Assisted Surgery

    Pre-Op THA Modelling

    • Recruiting
    • Age: 40 years and older
    • Surgery or procedure

    Replacing diseased hip joints with prosthetic implants in a procedure called total hip arthroplasty (THA) is associated with high rates of patient satisfaction, pain relief, and functional improvement when the implant is…

    Trial name
    NCT05221554
    Testing
    Imageless computer-navigated THA surgery, Standard of care THA surgery, CT-based Computer-navigated THA surgery
    Where
    Canada
    Volunteers
    180 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
  • Delirium - Postoperative

    Effects of PNB Timing on Postoperative Delirium for Hip Fracture

    • Not yet recruiting
    • Age: 65 to 100 years
    • Observational study
    • Surgery or procedure

    Hip fracture is a common cause of hospitalization in older adults and is associated with substantial pain and a high risk of delirium.

    Trial name
    NCT07856108
    Testing
    Peripheral Nerve Block for Hip Fracture
    Where
    Canada
    Volunteers
    120 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Completed, with results posted

All 11
  • Diabetic Ketoacidosis

    Intravenous Fluids in Adults With Diabetic Ketoacidosis in the Emergency Department

    • Completed
    • Age: 18 years and older
    • Results posted

    Diabetes mellitus is a common chronic disease. It is estimated that up to 40% of adults may develop diabetes in their lifetime. Patients with poorly controlled blood sugars often visit the emergency department for treatment of…

    Trial name
    BRISK-ED (NCT04926740)
    Testing
    Ringer's lactate
    Where
    Canada
    Volunteers
    74 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
    Can I take part? BRISK-ED
  • BPH, Depression

    5 Alpha Reductase Inhibitors And The Risk Of Suicide And Depression

    • Completed
    • Age: 66 to 120 years
    • Observational study
    • Results posted

    In December 2015, Health Canada issued a warning about a potential relationship between suicide and finasteride use and called for further research.

    Conditions
    BPH, Depression, Suicide
    Trial name
    NCT02876757
    Testing
    5ARI
    Volunteers
    186,394 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
    Can I take part? NCT02876757
  • Major Depressive Disorder

    Automatic Self Transcending Meditation Versus Treatment as Usual

    • Completed
    • Age: 60 to 85 years
    • Lifestyle or therapy programme
    • Results posted

    Depression is a leading contributor to global burden of disease. Antidepressants do not provide adequate response for many patients.

    Trial name
    NCT02149810
    Testing
    Automatic Self Transcending Meditation
    Where
    Canada
    Volunteers
    95 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
  • Urinary Tract Infection, Recurrent Urinary Tract Infection

    Effects of Antibiotic Prophylaxis on Recurrent UTI in Children

    • Completed
    • Age: 3 to 15 years
    • Phase 4
    • Results posted

    Approximately, 3% of males and 8% of females will develop a urinary tract infection (UTI) during childhood, and most of these will be effectively treated by short-term antibiotic therapy.

    Trial name
    NCT02357758
    Testing
    Antibiotic Prophylaxis
    Where
    Canada
    Volunteers
    59 people, healthy volunteers welcome
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
    Can I take part? NCT02357758
  • Chronic Rhinosinusitis, Aspirin Exacerbated Respiratory Disease

    Effect of Dietary Salicylate in Aspirin Exacerbated Respiratory Disease

    • Completed
    • Age: 18 to 100 years
    • Lifestyle or therapy programme
    • Results posted

    Aspirin-Exacerbated Respiratory Disease, or AERD, consists of aspirin sensitivity, asthma and nasal polyps. It is currently managed by chronic steroid use, multiple endoscopic sinus surgeries and/or aspirin desensitization.

    Conditions
    Chronic Rhinosinusitis, Aspirin Exacerbated Respiratory Disease, Asthma, Aspirin Sensitivity
    Trial name
    NCT01778465
    Testing
    Low salicylate diet, Normal Diet
    Where
    Canada
    Volunteers
    7 people
    Sponsor
    London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in