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10 Studies Recruiting

Clinical Trials Near Ottawa, Canada

Find research studies actively recruiting participants near Ottawa. Studies are run at established research institutions including Ottawa Hospital Research Institute and CHEO.

Top Research Institutions in Ottawa

1

Ottawa Hospital Research Institute

2

CHEO

Recruiting Studies Near Ottawa

#1

Physiology-guided vs Angiography-guided Non-culprit Lesion Complete Revascularization for Acute MI & Multivessel Disease

RECRUITINGNAPopulation Health Research Institute

COMPLETE-2 is a prospective, multi-centre, randomized controlled trial comparing a strategy of physiology-guided complete revascularization to angiography-guided complete revascularization in patients with acute ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI) and multivessel coronary artery disease (CAD) who have undergone successful culprit lesion Percutaneous Coronary Intervention (PCI). COMPLETE-2 OCT is a large scale, prospective, multi-centre, observational, imaging study of patients with STEMI or NSTEMI and multivessel CAD in a subset of eligible COMPLETE-2 patients.

๐Ÿ“ Los Angeles, California๐Ÿ“ San Francisco, California๐Ÿ“ Wichita, Kansas
#2

Brentuximab Vedotin in Early Stage Hodgkin Lymphoma

RECRUITINGPHASE3University College, London

RADAR is a multicentre, international, randomised, open-label phase III clinical trial composed of 2 trials running in parallel. Trial 1 will be led and sponsored by University College London (UCL) and conducted in Europe and Australia/New Zealand. Trial 2 will be led by the Canadian Cancer Trials Group (CCTG) and conducted in North America, with CCTG the regulatory sponsor in Canada, and University of Miami the regulatory sponsor and IND holder in the US. Datasets from Trial 1 and Trial 2 will be combined to achieve the total sample size. Data analysis will be performed by UCL and therefore UCL is responsible for the clinicaltrials.gov entry. Eligible patients will be randomised to receive either ABVD or A2VD chemotherapy. An interim PET-CT scan will be performed after 2 cycles of treatment, which will be used to adapt subsequent treatment. Patients will receive a total of 3-4 cycles of chemotherapy and may also receive involved site radiotherapy as consolidation. Patients will be followed up for a minimum of 5 years after treatment.

๐Ÿ“ Stanford, California๐Ÿ“ Miami, Florida๐Ÿ“ New York, New York
#3

Phase 2/3 Trial of Izalontamab Brengitecan vs Platinum-based Chemotherapy for Metastatic Urothelial Cancer With Disease Progression on or After Immunotherapy

RECRUITINGPHASE2, PHASE3Bristol-Myers Squibb

A Phase 2/3 Trial of Izalontamab Brengitecan vs Platinum-based Chemotherapy for Metastatic Urothelial Cancer with Disease Progression on or After Immunotherapy

๐Ÿ“ Palo Alto, California๐Ÿ“ Sacramento, California๐Ÿ“ Sacramento, California
#4

An Open-label Study Comparing Lutetium (177Lu) Vipivotide Tetraxetan Versus Observation in PSMA Positive OMPC.

RECRUITINGPHASE3Novartis Pharmaceuticals

The purpose of this study is to evaluate the efficacy and safety of lutetium (177Lu) vipivotide tetraxetan (AAA617) in participants with oligometastatic prostate cancer (OMPC) progressing after definitive therapy to their primary tumor. The data generated from this study will provide evidence for the treatment of AAA617 in early-stage prostate cancer patients to control recurrent tumor from progressing to fatal metastatic disease while preserving quality of life by delaying treatment with androgen deprivation therapy (ADT).

๐Ÿ“ Fayetteville, Arkansas๐Ÿ“ Los Angeles, California๐Ÿ“ Palo Alto, California
#5

CONCEPTT Kids International Neurodevelopmental Outcomes Among Offspring of Women With Type 1 Diabetes

RECRUITINGNot SpecifiedUniversity of Manitoba

Neurodevelopmental Outcomes among Offspring of women with Type 1 Diabetes: A Follow up Study of the CONCEPTT Randomized Control Trial (CONCEPTT Kids International). An international, multicentre prospective cohort study of child and mother pairs. The potential number of recruits is 225 and the main inclusion criteria is child's mother who participated in the CONCEPTT Trial.

๐Ÿ“ Calgary, Alberta๐Ÿ“ Halifax, Nova Scotia๐Ÿ“ Ottawa, Ontario
#6

A Study to Evaluate ALN-HTT02 in Adult Patients With Huntington's Disease

RECRUITINGPHASE1Alnylam Pharmaceuticals

The purpose of this study is to evaluate the safety, tolerability, pharmacodynamics (PD) and pharmacokinetics (PK) of single or repeat doses of ALN-HTT02.

๐Ÿ“ Edmonton๐Ÿ“ Montreal๐Ÿ“ Ottawa
#7

Laplace Early Feasibility Study - Canada

RECRUITINGNALaplace Interventional, Inc

The objective of the study is to assess the safety and technical feasibility of the Laplace Transcatheter Tricuspid Valve Replacement (TTVR) System

๐Ÿ“ Ottawa, Ontario๐Ÿ“ Toronto, Ontario๐Ÿ“ Toronto, Ontario
#8

A Study to Compare Standard Therapy to Treat Hodgkin Lymphoma to the Use of Two Drugs, Brentuximab Vedotin and Nivolumab

RECRUITINGPHASE3National Cancer Institute (NCI)

This phase III trial compares the effect of adding immunotherapy (brentuximab vedotin and nivolumab) to standard treatment (chemotherapy with or without radiation) to the standard treatment alone in improving survival in patients with stage I and II classical Hodgkin lymphoma. Brentuximab vedotin is in a class of medications called antibody-drug conjugates. It is made of a monoclonal antibody called brentuximab that is linked to a cytotoxic agent called vedotin. Brentuximab attaches to CD30 positive lymphoma cells in a targeted way and delivers vedotin to kill them. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Chemotherapy drugs such as doxorubicin hydrochloride, bleomycin sulfate, vinblastine sulfate, dacarbazine, and procarbazine hydrochloride work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Cyclophosphamide is in a class of medications called alkylating agents. It works by damaging the cell's deoxyribonucleic acid (DNA) and may kill cancer cells. It may also lower the body's immune response. Etoposide is in a class of medications known as podophyllotoxin derivatives. It blocks a certain enzyme needed for cell division and DNA repair and may kill cancer cells. Vincristine is in a class of medications called vinca alkaloids. It works by stopping cancer cells from growing and dividing and may kill them. Prednisone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response to help lessen the side effects of chemotherapy drugs. Radiation therapy uses high energy x-rays to kill tumor cells and shrink tumors. Adding immunotherapy to the standard treatment of chemotherapy with or without radiation may increase survival and/or fewer short-term or long-term side effects in patients with classical Hodgkin lymphoma compared to the standard treatment alone.

๐Ÿ“ Birmingham, Alabama๐Ÿ“ Mobile, Alabama๐Ÿ“ Anchorage, Alaska
#9

Evaluating Dose Timing (Morning vs Evening) of Endocrine-based Therapies in Metastatic Breast and Prostate Cancers

RECRUITINGPHASE4Ottawa Hospital Research Institute

The REaCT-CHRONO-MetBP Pilot study will compare morning and evening administration of endocrine-based therapy in metastatic breast and prostate cancers. Participants with metastatic breast or prostate cancer will be randomly placed in one of two groups: a morning group and an evening group. The group assignment will determine whether they take their endocrine therapy in the morning or the evening. The primary outcome of this pilot study is to evaluate the feasibility of study procedures in order to conduct a larger definitive trial in the future. The secondary outcomes include comparing quality of life, tolerability, and efficacy outcomes between the morning and evening groups for each of the two cancer cohorts (metastatic breast and prostate cancer).

๐Ÿ“ Kitchener, Ontario๐Ÿ“ Ottawa, Ontario
#10

PromotIng Optimal Treatment for Community-acquired PNeumonia in EmErgency Rooms

RECRUITINGNAJeffrey Pernica

In North America, up to 5% of preschoolers develop community-acquired pneumonia (CAP) every year. Pneumonia is the second-leading reason for paediatric hospitalization in both Canada and the US; approximately 20% of children hospitalized with CAP may need intensive care, which can result in significant morbidity. Given this burden of disease, it is critical that CAP is managed appropriately. Specific therapy for CAP is dependent on microbiologic aetiology, as bacterial disease will improve with antibiotic treatment.

๐Ÿ“ Calgary, Alberta๐Ÿ“ Ottawa, Ontario

Clinical Trials in Ottawa: FAQ

How do I find clinical trials near Ottawa?

Corterve aggregates all actively recruiting clinical trials near Ottawa, Canada from the ClinicalTrials.gov database. Simply browse the listings on this page or take our free health assessment to find trials you may qualify for.

Are clinical trials in Ottawa free?

Yes, clinical trials are free for participants. The research sponsor covers all study-related costs. Many trials near Ottawa, Canada also provide compensation for your time and travel expenses.

What research institutions are located in Ottawa?

Ottawa is home to several leading research institutions, including Ottawa Hospital Research Institute, CHEO. These facilities run clinical trials across Oncology, Neurology, Cardiology, and other therapeutic areas.

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