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Saving Residual Renal Function Among Haemodialysis Patients Receiving Irbesartan (SAFIR)

Primary Purpose

Kidney Failure, Chronic

Status
Completed
Phase
Phase 3
Locations
Denmark
Study Type
Interventional
Intervention
Irbesartan
Placebo matching irbesartan 150 mg
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Kidney Failure, Chronic focused on measuring Residual renal function, Haemodialysis, Applanation tonometry, Cardiac output, Quality of life, Angiotensin II Type 1 Receptor Blockers

Eligibility Criteria

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

Inclusion Criteria:

  • Haemodialysis patient
  • Haemodialysis treatment for maximum 12 months
  • > 18 years old
  • informed consent
  • urine volume > 300 ml / 24 hours
  • contraception if fertile woman

Exclusion Criteria:

  • Systolic blood pressure < 110 mm Hg
  • Able to comprehend the aims of the project and follow instructions
  • Allergy to irbesartan/ACE-inhibitors/ARBs
  • Myocardial infarction or unstable angina pectoris during the last 3 months
  • Ejection fraction < 30 %
  • Pregnancy

Sites / Locations

  • Department of Nephrology, Aarhus University, Aalborg
  • Department of Nephrology, Aarhus University Hospital, Skejby
  • Department of Medicine, Fredericia Hospital
  • Haemodialysis unit, Horsens Hospital
  • Hemodialysis Unit, Randers Hospital
  • Department of Medicine M, Viborg Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Irbesartan

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Decrease in loss of residual kidney function.

Secondary Outcome Measures

Cardio-vascular outcome assessed by applanation tonometry, echocardiography, Transonic measurements of cardiac output and markers in blood.
Progression to anuria
Quality of life assessed by a questionnaire: Kidney Disease Quality Of Life - Short Form (KDQOL-SF)

Full Information

First Posted
November 14, 2008
Last Updated
January 7, 2013
Sponsor
University of Aarhus
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1. Study Identification

Unique Protocol Identification Number
NCT00791830
Brief Title
Saving Residual Renal Function Among Haemodialysis Patients Receiving Irbesartan
Acronym
SAFIR
Official Title
Saving Residual Renal Function Among Haemodialysis Patients Receiving Irbesartan - a Double Blind Randomised Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
April 2009 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
January 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Angiotensin II receptor blockers (ARB) are known to preserve kidney function among patients with kidney diseases and reduced renal function, but not among haemodialysis patients. Haemodialysis patients often lose residual renal function after initiating dialysis leading to worsened quality of life, increased morbidity and mortality. In this study an ARB is investigated in a double blind, randomised, parallel group, placebo controlled manner to see, if this ARB can save residual renal function among haemodialysis patients. Potential cardiovascular benefits of the treatment are also addressed.
Detailed Description
Haemodialysis patients often lose residual renal function rather quickly after initiation of dialysis - average loss is 30 % per year. Loss of residual kidney function leads to deteriorating quality of life, more morbidity and a higher mortality. Many causes to this has been identified, but no one has - to my knowledge - addressed saving of residual renal function among haemodialysis patients so far. Hypothesis: Irbesartan can reduce loss of residual kidney function among haemodialysis patients and left ventricular hypertrophy and arterial stiffness is less pronounced after 1 year of treatment. Methods: 80 patients are randomised to receive either irbesartan, an angiotensin II receptor blocker (ARB), or placebo for 1 year. Residual renal function will be estimated before and one-two weeks after initiating project medicine, in order to estimate the acute effect of ARB on residual renal function in this study population. Thereafter, glomerular filtration rate (GFR) and urine volume will be determined after 3, 6, 9 and 12 months giving a regression line for each patient. 8 dialysis units will be recruiting patients. Investigations: creatinine-urea-clearance by 24h urine collection applanation tonometry cardiac output echocardiography QoL questionnaire endocrinological and cardiovascular markers in blood and urine Perspectives: It is well-known that ceased urine production has a tremendous negative effect on the quality of life of haemodialysis patients. Lately it was shown that residual renal function has greater impact than dialysis dose on morbidity as well as mortality. Among peritoneal dialysis patients in Asia an angiotensin-converting enzyme inhibitors (ACEI) or an ARB saved residual renal function, but preservation of renal function has not been addressed in haemodialysis patients, and ACEI or ARB are only prescribed to roughly 15 % of these. If this study confirms our hypothesis the growing population of haemodialysis patients should be offered irbesartan.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Failure, Chronic
Keywords
Residual renal function, Haemodialysis, Applanation tonometry, Cardiac output, Quality of life, Angiotensin II Type 1 Receptor Blockers

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
82 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Irbesartan
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Irbesartan
Other Intervention Name(s)
Aprovel, Karvea, Avapro, CAS no: 138402-11-6, ATC code: C09CA04, PubChem: 3749, Drugbank: APRD00413
Intervention Description
Tablets, 300 mg * 1 daily, 1 year
Intervention Type
Drug
Intervention Name(s)
Placebo matching irbesartan 150 mg
Intervention Description
Tablets, 300 mg * 1 daily, 1 year
Primary Outcome Measure Information:
Title
Decrease in loss of residual kidney function.
Time Frame
3, 6, 9 and 12 months
Secondary Outcome Measure Information:
Title
Cardio-vascular outcome assessed by applanation tonometry, echocardiography, Transonic measurements of cardiac output and markers in blood.
Time Frame
1 year
Title
Progression to anuria
Time Frame
3, 6, 9 and 12 months
Title
Quality of life assessed by a questionnaire: Kidney Disease Quality Of Life - Short Form (KDQOL-SF)
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Haemodialysis patient Haemodialysis treatment for maximum 12 months > 18 years old informed consent urine volume > 300 ml / 24 hours contraception if fertile woman Exclusion Criteria: Systolic blood pressure < 110 mm Hg Able to comprehend the aims of the project and follow instructions Allergy to irbesartan/ACE-inhibitors/ARBs Myocardial infarction or unstable angina pectoris during the last 3 months Ejection fraction < 30 % Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bente Jespersen, MD, DrMedSc
Organizational Affiliation
Department of Nephrology, Aarhus University Hospital, Skejby, Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Erik Sloth, MD, DrMedSc
Organizational Affiliation
Department of Anaesthesiology and Intensive Care, Aarhus University Hospital, Skejby, Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jens Kristian D Jensen, MD, PhD
Organizational Affiliation
Department of Nephrology, Aarhus University Hospital, Skejby, Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Krista D Kjærgaard, MD, PhD
Organizational Affiliation
Department of Nephrology, Aarhus University Hospital, Skejby, Denmark
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Christian D Peters, MD
Organizational Affiliation
Department of Nephrology, Aarhus University Hospital, Skejby, Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Charlotte Strandhave, MD
Organizational Affiliation
Department of Nephrology, Aalborg University Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ida N Tietze, MD, PhD
Organizational Affiliation
Department of Internal Medicine, Region Hospital Viborg, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marija K Novosel, MD
Organizational Affiliation
Department of Internal Medicine, Region Hospital Fredericia, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Nephrology, Aarhus University, Aalborg
City
Aalborg
ZIP/Postal Code
9000
Country
Denmark
Facility Name
Department of Nephrology, Aarhus University Hospital, Skejby
City
Aarhus N
ZIP/Postal Code
8200
Country
Denmark
Facility Name
Department of Medicine, Fredericia Hospital
City
Fredericia
ZIP/Postal Code
7000
Country
Denmark
Facility Name
Haemodialysis unit, Horsens Hospital
City
Horsens
ZIP/Postal Code
8700
Country
Denmark
Facility Name
Hemodialysis Unit, Randers Hospital
City
Randers
ZIP/Postal Code
8600
Country
Denmark
Facility Name
Department of Medicine M, Viborg Hospital
City
Viborg
ZIP/Postal Code
8800
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
33115436
Citation
Peters CD, Kjaergaard KD, Christensen KL, Bibby BM, Jespersen B, Jensen JD. High-sensitivity Troponin T in hemodialysis patients: a randomized placebo-controlled sub-study investigating angiotensin-II-blockade, variation over time and associations with clinical outcome. BMC Nephrol. 2020 Oct 28;21(1):452. doi: 10.1186/s12882-020-02103-1.
Results Reference
derived
PubMed Identifier
26030651
Citation
Peters CD, Kjaergaard KD, Jensen JD, Christensen KL, Strandhave C, Tietze IN, Novosel MK, Bibby BM, Jespersen B. Short and Long-Term Effects of the Angiotensin II Receptor Blocker Irbesartan on Intradialytic Central Hemodynamics: A Randomized Double-Blind Placebo-Controlled One-Year Intervention Trial (the SAFIR Study). PLoS One. 2015 Jun 1;10(6):e0126882. doi: 10.1371/journal.pone.0126882. eCollection 2015.
Results Reference
derived
PubMed Identifier
23651713
Citation
Peters CD, Kjaergaard KD, Jespersen B, Christensen KL, Jensen JD. Renal and cardiovascular effects of irbesartan in dialysis patients--a randomized controlled trial protocol (SAFIR study). Dan Med J. 2013 Apr;60(4):A4602.
Results Reference
derived

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Saving Residual Renal Function Among Haemodialysis Patients Receiving Irbesartan

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