We are seeking those with lived experience in nephrology care of all ages from all corners of the country to join the Capacity Building and Communications and Engagement Committees of the Canadian Nephrology Trials Network.

Females living with kidney disease are invited to complete a voluntary, anonymous survey about their beliefs, perceptions and priorities regarding reproductive health and kidney disease.

Identifying what is most important to people with kidney failure as they have surgery, to learn more about these outcomes and understand if tools should be developed to predict the risk of those outcomes.

Collecting valuable information from health care practitioners and patient partners about experiences and challenges faced when treating Acute Kidney Injury. This information will be used to develop a set of accessible and practical resources for family doctors and patients to help improve the AKI care.

Seeking patient partners to identify mental health concerns, including those among Indigenous individuals receiving hemodialysis.

We are looking for people like you or “patient partners” to co-create an app to help those receiving in-center hemodialysis live, feel, and be well.

Looking for patient partners to help us develop a video to highlight the patient experience on topics related to deprescribing and participation in kidney research.

Join other people living with chronic kidney disease and learn from a team of wellness and kidney experts.

Participants are invited to complete a 15-minute survey with questions about their experience with kidney care in Alberta.

The purpose of this study is to determine if spironolactone reduces death or hospitalization for heart failure and is well tolerated in patients that require dialysis.