Actively Recruiting
Targeted Deprescribing in Patients on Hemodialysis
Led by University Health Network, Toronto · Updated on 2024-12-13
480
Participants Needed
4
Research Sites
182 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Hemodialysis (HD) patients take more pills per day on average than any other chronically ill patient population. On average, an HD patient takes 19 medications per day, of which 70% may not be appropriate. The reason the medications may not be appropriate is that HD patients are rarely included in clinical trials for new medications and therefore the efficacy and safety data that exists for the general population may not actually apply to them. Tools to guide the re-assessment and discontinuation (deprescribing) of these specific medications that lack evidence for efficacy and safety in HD patients are needed. These tools will help reduce the amount of medications being taken and the potential negative consequences of taking so many medications (e.g. adverse drug reactions, drug interactions, non-adherence, increased risk of cognitive impairment, impaired balance and falls, and increased risk of morbidity, hospitalization, and mortality). Nine medications that are often inappropriately prescribed to HD patients have been identified by the investigators. These medications are: Alpha-1 Blockers, Anticonvulsants, Benzodiazepines \& Z-Drugs, Loop Diuretics, Prokinetic Agents, Proton Pump Inhibitors, Quinine, Urate Lowering Agents, and Statins. The investigators developed and validated tools to help medical teams in outpatient HD units with identifying and stopping these medications in their patients. The next step will be to perform a study where test these tools are tested in practice at multiple HD centers across Canada. This initiative should decrease the average number of medications per patient and inappropriate medication use in the HD units where these tools are used. The overall objective of this study is to improve current clinical practice by optimizing medication use and prescribing patterns in the HD units across Canada.
CONDITIONS
Official Title
Targeted Deprescribing in Patients on Hemodialysis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18+ years
- Receiving outpatient hemodialysis treatment at one of the four study sites for at least the past three months
- Able to read and understand English and provide consent
You will not qualify if you...
- Acute starts to hemodialysis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
Providence Health Care
Vancouver, British Colombia, Canada, V6Z 1Y6
Active, Not Recruiting
2
Manitoba Renal Program
Winnipeg, Manitoba, Canada, R2V 3M3
Active, Not Recruiting
3
Nova Scotia Health Authority
Halifax, Nova Scotia, Canada
Active, Not Recruiting
4
University Health Network
Toronto, Ontario, Canada, M5G 2C4
Actively Recruiting
Research Team
M
Marisa Battistella, PharmD
CONTACT
M
Melissa Lefebvre, MBiotech
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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