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Trial registered on ANZCTR
Registration number
ACTRN12608000016336
Ethics application status
Approved
Date submitted
10/01/2008
Date registered
14/01/2008
Date last updated
15/07/2010
Type of registration
Prospectively registered
Titles & IDs
Public title
Ascorbate Supplementation in Kidney Failure
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Scientific title
Ascorbate supplementation in Kidney failure and effect on quality of life
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Secondary ID [1]
252228
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Vitamin C supplementation in kidney failure: effect on uraemic symptoms
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Renal Failure
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Condition category
Condition code
Renal and Urogenital
2821
2821
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0
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Kidney disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Oral ascorbic acid 250mg three times a week for 3 months from when subject is first enrolled into the study
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Intervention code [1]
2438
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Treatment: Drugs
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Comparator / control treatment
placebo, the exact formulation of the placebo is yet to be determined but will be of a simlar size and taste to the active treatment, with the same dosage schedule (orally three times a week for 3 months).
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Kidney diseases quality of life short form symptom subscale score
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Assessment method [1]
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Timepoint [1]
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3 months from when subject is first enrolled into the study
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Primary outcome [2]
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Kidney quality of life short form cognitive subscale
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Assessment method [2]
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Timepoint [2]
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3 months from when subject is first enrolled into the study
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Secondary outcome [1]
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Haemodialysis cardiovascular instability. As determined by the need for fluid bolus, slowwing of ultrafiltration rate or "head down" positioning
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Assessment method [1]
6249
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Timepoint [1]
6249
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at each dialysis episode which will usually be 3 times per week for three months from when subject is first enrolled into the study
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Eligibility
Key inclusion criteria
Receiving maintenance dialysis treatment OR estimated Modification of Diet in Renal Diseases Glomerular Filtration Rate (MDRD GFR) of less than 20ml/min
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Life expectancy less than 3 months
Primary hyperoxaluria
Clinically unstable
Unable to provide informed consent
Unwilling to cease non study ascorbate containing supplements
Not fluent in English
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
central randomisation
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
stratified by diabetic and dialysis status
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/06/2008
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
100
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment postcode(s) [1]
543
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2605
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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The Canberra Hospital Private Practice FundFunding
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Address [1]
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The Canberra Hospital Private Practice Fund, The Canberra Hospital, 77 Yamba Drive, Garran, ACT 2611, Australia
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Country [1]
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Australia
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Primary sponsor type
Hospital
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Name
The Canberra Hospital
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Address
77 Yamba Drive
Garran
ACT 2605
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
2667
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Country [1]
2667
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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ACT Health Human Ethics Research Committee
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Ethics committee address [1]
4895
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11 Moore St, Canberra City
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Ethics committee country [1]
4895
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Date submitted for ethics approval [1]
4895
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02/05/2008
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Approval date [1]
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01/07/2008
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Ethics approval number [1]
4895
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ETH.5/08.491
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Summary
Brief summary
The primary aim of this study is to discover if giving patients with severe kidney failure ascorbate (vitamin C) reduces symptoms that are common to both renal failure and ascorbate deficiency. It is known that low ascorbate levels are common in patients with severe kidney failure, and that symptoms of scurvy (ascorbate deficiency) and of kidney failure (uraemic syndrome) overlap. There is however no consensus on whether ascorbate supplementation is beneficial in patients with severe kidney disease and there are concerns that supplementation may cause adverse effects. This study would significantly improve clinical care, by examining the benefits and adverse outcomes of supplementation.
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Trial website
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Trial related presentations / publications
Nephrology Dialysis Transplantation 2010; doi: 10.1093/ndt/gfq412
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Richard Singer
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Address
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The Canberra Hospital Renal Service
Level 8, Building 1
77 Yamba Drive
Garran
ACT 2605
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Country
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Australia
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Phone
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+61262242222
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Fax
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+61262443281
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Email
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[email protected]
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Contact person for scientific queries
Name
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Richard Singer
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Address
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The Canberra Hospital Renal Service
Level 8, Building 1
77 Yamba Drive
Garran
ACT 2605
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Country
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Australia
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Phone
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+61262442222
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Fax
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+61262443281
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Interventions for fatigue in people with kidney failure requiring dialysis.
2023
https://dx.doi.org/10.1002/14651858.CD013074.pub2
N.B. These documents automatically identified may not have been verified by the study sponsor.
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