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Eplerenone in Hemodialysis Trial (PHASE)

Primary Purpose

Hemodialysis, End Stage Renal Disease

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
eplerenone
Placebo
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemodialysis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥18 years
  • On hemodialysis >90 days
  • Prescribed target body weight within 1 kg of current for all dialysis sessions within 4 weeks prior to randomization
  • Able to provide written informed consent to participate

Exclusion Criteria:

  • Occurrence of documented clinically important hypotension (systolic blood pressure <90 that required treatment) within 4 weeks of randomization
  • Change in blood pressure medications within 4 weeks prior to randomization
  • Occurrence of pre-dialysis serum potassium >6.0 mmol/L in 4 weeks prior to randomization
  • Currently treated with and cannot withdraw spironolactone or eplerenone due to medical necessity
  • Known allergy or sensitivity to eplerenone
  • Pregnancy
  • Scheduled living related donor renal transplant within the next 6 months

Sites / Locations

  • St. Joseph's Healthcare
  • St. Michael's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Eplerenone

Placebo

Arm Description

Target of 50 mg/day

Matching placebo

Outcomes

Primary Outcome Measures

permanent discontinuation of the study medication for hyperkalemia or permanent discontinuation of the study medication for hyperkalemia or hypotension

Secondary Outcome Measures

permanent discontinuation of study drug for any reason
treatment adherence
pre-dialysis potassium
frequency of serious adverse events
frequency of hospitalizations for a vascular reason
fatal and non-fatal vascular events

Full Information

First Posted
July 23, 2012
Last Updated
September 24, 2015
Sponsor
McMaster University
Collaborators
Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT01650012
Brief Title
Eplerenone in Hemodialysis Trial
Acronym
PHASE
Official Title
Pilot Trial of Hemodialysis Patient Aldosterone antagoniSm With Eplerenone Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Forty percent of patients that require dialysis for kidney failure die within three years mostly due to heart disease. Heart failure and high blood pressure are common problems in patients that require dialysis and are key causes of death due to heart disease. Eplerenone is a drug that is very effective at improving heart failure and reducing blood pressure in patients that do not require dialysis. There is currently no evidence to tell physicians whether eplerenone would have similar benefits in patients that require dialysis. This evidence can only be reliably generated by performing a large scale study. Before such a study is undertaken, the investigators must determine whether eplerenone will be well tolerated and safe in patients that require dialysis. The investigators will perform an initial small trial called the Pilot trial in Hemodialysis patients undergoing Aldosterone antagoniSm with Eplerenone (PHASE) to determine if eplerenone is a well tolerated, safe medication to use in a very large, global study that will show whether or not eplerenone reduces important outcomes for patients like death from heart causes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemodialysis, End Stage Renal Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
158 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Eplerenone
Arm Type
Experimental
Arm Description
Target of 50 mg/day
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Matching placebo
Intervention Type
Drug
Intervention Name(s)
eplerenone
Intervention Description
target 50 mg per day titrated down for hyperkalemia or hypotension
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
permanent discontinuation of the study medication for hyperkalemia or permanent discontinuation of the study medication for hyperkalemia or hypotension
Time Frame
13 weeks
Secondary Outcome Measure Information:
Title
permanent discontinuation of study drug for any reason
Time Frame
13 weeks
Title
treatment adherence
Time Frame
13 weeks
Title
pre-dialysis potassium
Time Frame
13 weeks
Title
frequency of serious adverse events
Time Frame
13 weeks
Title
frequency of hospitalizations for a vascular reason
Time Frame
13 weeks
Title
fatal and non-fatal vascular events
Time Frame
13 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years On hemodialysis >90 days Prescribed target body weight within 1 kg of current for all dialysis sessions within 4 weeks prior to randomization Able to provide written informed consent to participate Exclusion Criteria: Occurrence of documented clinically important hypotension (systolic blood pressure <90 that required treatment) within 4 weeks of randomization Change in blood pressure medications within 4 weeks prior to randomization Occurrence of pre-dialysis serum potassium >6.0 mmol/L in 4 weeks prior to randomization Currently treated with and cannot withdraw spironolactone or eplerenone due to medical necessity Known allergy or sensitivity to eplerenone Pregnancy Scheduled living related donor renal transplant within the next 6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Walsh
Organizational Affiliation
McMaster University, Population Health Research Institute, St. Joseph's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ron Wald
Organizational Affiliation
Keenan Research Centre, St. Michael's Hospital, University of Toronto
Official's Role
Principal Investigator
Facility Information:
City
Calgary
State/Province
Alberta
Country
Canada
City
Winnipeg
State/Province
Manitoba
Country
Canada
Facility Name
St. Joseph's Healthcare
City
Hamilton
State/Province
Ontario
Country
Canada
City
London
State/Province
Ontario
Country
Canada
Facility Name
St. Michael's Hospital
City
Toronto
State/Province
Ontario
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
33586138
Citation
Hasegawa T, Nishiwaki H, Ota E, Levack WM, Noma H. Aldosterone antagonists for people with chronic kidney disease requiring dialysis. Cochrane Database Syst Rev. 2021 Feb 15;2(2):CD013109. doi: 10.1002/14651858.CD013109.pub2.
Results Reference
derived

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Eplerenone in Hemodialysis Trial

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