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Mineralocorticoid Receptor Antagonist
Spironolactone for Kidney Failure (ACHIEVE Trial)
Phase 3
Recruiting
Led By Michael Walsh, MD, PhD
Research Sponsored by Population Health Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age ≥45 years or ≥18 with a history of diabetes
On hemodialysis prescribed at least 2 treatments per week or on peritoneal dialysis prescribed with at least 1 exchange daily
Must not have
Currently taking and unable to withdraw a mineralocorticoid receptor antagonist (i.e. spironolactone or eplerenone)
Scheduled living related donor renal transplant
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
All Individual Drugs Already Approved
Approved for 10 Other Conditions
Pivotal Trial
Summary
This trial tests if spironolactone, a pill that blocks a harmful hormone, can reduce heart problems in dialysis patients. These patients are at high risk of heart failure and death, and the pill aims to lower blood pressure and protect their hearts. Spironolactone has been shown to effectively lower blood pressure in patients with resistant hypertension.
Who is the study for?
This trial is for adults on dialysis due to kidney failure, who've been receiving treatment for at least 90 days. It's open to those aged 45 and above or adults over 18 with diabetes. Participants must not be pregnant, breastfeeding, have high potassium levels, known allergies to spironolactone, or be in another similar drug trial.
What is being tested?
The study tests if Spironolactone can reduce heart failure and related deaths in patients on dialysis. Half of the participants will receive Spironolactone while the other half will get a placebo (a pill with no active drug), to compare outcomes between the two groups.
What are the potential side effects?
Spironolactone may cause side effects like increased potassium levels which can affect heart rhythm, breast enlargement in men, menstrual irregularities in women, dehydration symptoms such as dry mouth/thirsty feeling or muscle cramps.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am at least 45 years old or I am 18 or older with diabetes.
Select...
I am on dialysis, either hemodialysis twice a week or peritoneal dialysis daily.
Select...
I have been on dialysis for at least 90 days.
Select...
I am on dialysis, either hemodialysis twice a week or peritoneal dialysis daily.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am currently on a medication like spironolactone or eplerenone and cannot stop.
Select...
I am scheduled for a kidney transplant from a living relative.
Select...
I am not in a trial for drugs that interact with spironolactone.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 10 Other Conditions
This treatment demonstrated efficacy for 10 other conditions.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Spironolactone 25 MG TabletActive Control1 Intervention
25 mg of active spironolactone in tablet form
Group II: Placebo Oral TabletPlacebo Group1 Intervention
A tablet with no active medication that will be an exact match of the active spironolactone in taste and appearance
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Aldosterone blockers, such as spironolactone, work by inhibiting the action of aldosterone, a hormone that increases sodium and water retention, leading to high blood pressure and further kidney damage. By blocking aldosterone, these medications help reduce blood pressure and prevent fluid overload, which is crucial for patients with kidney failure to avoid complications like heart failure.
Other common treatments include ACE inhibitors and ARBs, which also lower blood pressure and reduce proteinuria, thereby slowing the progression of kidney disease. Sodium-glucose co-transporter 2 (SGLT2) inhibitors are another class that helps reduce glucose reabsorption in the kidneys, lowering blood sugar levels and providing renal protection.
These treatments are vital for managing symptoms and slowing the progression of kidney failure, improving patient outcomes.
Effect of mineralocorticoid receptor antagonists on proteinuria and progression of chronic kidney disease: a systematic review and meta-analysis.
Effect of mineralocorticoid receptor antagonists on proteinuria and progression of chronic kidney disease: a systematic review and meta-analysis.
Find a Location
Who is running the clinical trial?
Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,388 Previous Clinical Trials
26,515,323 Total Patients Enrolled
2 Trials studying Kidney Failure
398 Patients Enrolled for Kidney Failure
Population Health Research InstituteLead Sponsor
164 Previous Clinical Trials
715,764 Total Patients Enrolled
Michael Walsh, MD, PhDPrincipal InvestigatorMcMaster University
2 Previous Clinical Trials
224 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am at least 45 years old or I am 18 or older with diabetes.My doctor says I must or must not take spironolactone.I am currently on a medication like spironolactone or eplerenone and cannot stop.I am scheduled for a kidney transplant from a living relative.The doctor thinks you have less than 6 months to live.I am not in a trial for drugs that interact with spironolactone.I am on dialysis, either hemodialysis twice a week or peritoneal dialysis daily.I have been on dialysis for at least 90 days.You are allergic to spironolactone.I am on dialysis, either hemodialysis twice a week or peritoneal dialysis daily.Your blood potassium levels have been too high in the past six weeks or during the study's initial phase.
Research Study Groups:
This trial has the following groups:- Group 1: Placebo Oral Tablet
- Group 2: Spironolactone 25 MG Tablet
Awards:
This trial has 3 awards, including:- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
- Approved for 10 Other Conditions - This treatment demonstrated efficacy for 10 other conditions.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
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.
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