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Medication Reduction for Aging
Phase 4
Waitlist Available
Led By Scott Garrison, MD, PhD
Research Sponsored by University of Alberta
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
≥80 years of age
Using ≥6 long-term oral medications (defined as orally administered medications dispensed ≥2 times in the preceding 200 days)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an expected average of 2 years
Awards & highlights
Study Summary
This trial is designed to study whether reducing the number of medications that older adults take will improve their health outcomes.
Who is the study for?
This trial is for individuals who are 80 years or older, take six or more long-term oral medications, see participating primary care providers regularly, and live independently (not in a nursing home). There are no specific exclusion criteria.Check my eligibility
What is being tested?
The study tests if reducing medication doses can benefit seniors. It involves reviewing patients' current medications to find the lowest effective doses for symptom relief and adjusting drugs that control blood pressure and sugar to safer levels.See study design
What are the potential side effects?
Since the intervention involves lowering medication dosages already prescribed, side effects may include changes in how well symptoms are managed. However, this approach aims to reduce adverse drug reactions common in older adults.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 80 years old or older.
Select...
I am taking 6 or more long-term oral medications.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an expected average of 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an expected average of 2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Composite of all-cause mortality or nursing home admission
Secondary outcome measures
Acute care costs
All-cause mortality
All-cause unplanned hospitalization or emergency room visit
+13 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Medication minimizationExperimental Treatment1 Intervention
Patients have a dedicated medication minimization visit with their usual primary care provider to which they bring all of their medications (a so-called "brown bag" medication review).
Group II: Usual CareActive Control1 Intervention
Patients will continue to receive care as appropriate but no dedicated visit to review and minimize medications will be organized as a result of the study. Medications are free to be minimized during the normal course of care should the need arise.
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Who is running the clinical trial?
University of AlbertaLead Sponsor
886 Previous Clinical Trials
382,978 Total Patients Enrolled
3 Trials studying Frailty
591 Patients Enrolled for Frailty
Scott Garrison, MD, PhDPrincipal InvestigatorUniversity of Alberta
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am 80 years old or older.I am taking 6 or more long-term oral medications.Not applicable.
Research Study Groups:
This trial has the following groups:- Group 1: Usual Care
- Group 2: Medication minimization
Awards:
This trial has 3 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Has the FDA sanctioned medication reduction as a viable medical approach?
"Given the fact that this medication is approved, our team at Power has assigned a score of 3 to signify its safety."
Answered by AI
Are there still openings available for patients to take part in this trial?
"Data from clinicaltrials.gov indicates that enrollment in this trial has closed as of August 2nd 2022. Although, there are 380 alternative trials with open recruitment processes available to interested participants at present."
Answered by AI
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