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Trace Element Replenishment Study in Hemodialysis Patients

Trace Element Replenishment Study in Hemodialysis Patients

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01473914
Enrollment
150
Registered
2011-11-17
Start date
2012-11-30
Completion date
2014-01-31
Last updated
2016-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End Stage Renal Disease

Brief summary

A pilot randomized trial that compares a new renal nutritional supplement with the standard renal vitamin. The primary objective is to compare two doses (medium and high) of the new supplement with the renal vitamin currently being prescribed to people with End Stage Renal Disease (ESRD). Secondary objective is to demonstrate the feasibility of recruitment for a definitive larger trial.

Detailed description

People with severe kidney disease follow a restricted diet aimed at reducing intake of sodium, potassium and phosphate. These dietary restrictions require reducing their intake of many fresh fruits and vegetables, which may lead to nutritional deficiency. Although the potential for malnutrition in people with kidney disease is well recognized, blood levels of most vitamins and trace elements are rarely measured. Instead, most North Americans with severe kidney disease are routinely prescribed a renal vitamin such as Replavite which contains a mixture of B and C vitamins. Recent evidence (including our work; see http://www.biomedcentral.com/bmcmed/subjects/nephrology) indicates that people with severe kidney disease are often deficient in several other biologically essential substances (selenium, zinc) that are readily amenable to supplementation. Pilot data from the Northern Alberta Renal Program (NARP) indicate that approximately 90% of patients have zinc levels below the lower limit of normal; findings for selenium are similar. Potential benefits of zinc supplementation include improvements in immune function, taste sensitivity (perhaps reducing dietary sodium intake), and improved appetite. Potential benefits of selenium supplementation include reductions in the risk of vascular disease and infection. Supplementation with vitamin E was shown in a randomized trial to reduce serious cardiovascular morbidity in people with kidney failure, but is not routinely used in dialysis patients. This suggests that supplementation of zinc, selenium, and vitamin E has theoretical benefits in kidney failure. Since patients with kidney failure already take many medications, it is logical to combine any new nutritional supplements with the ingredients of the standard renal vitamin to reduce pill burden. This protocol concerns a novel nutritional supplement consisting of zinc, selenium and vitamin E in addition to the contents of the standard renal supplement of B and C vitamins. This pilot randomized, double blind trial will compare 2 doses of the new supplement with the standard renal vitamin. 2.0 Objectives: Primary objective: compare two formulations of the new supplement (low and medium doses of zinc and selenium) with standard treatment (Replavite or equivalent renal vitamin). Secondary objective: demonstrate the feasibility of recruitment for a definitive larger trial

Interventions

DIETARY_SUPPLEMENTLow dose: supplemental zinc, selenium and vitamin E

1. ZINC 25mg (AS ZINC SULFATE) 2. SELENIUM 50 mcg (AS SODIUM SELENITE) 3. VITAMIN E (D-ALPHA-TOCOPHEROL) (AS SUCCINATE) 250 IU

DIETARY_SUPPLEMENTStandard renal vitamin: B and C renal vitamin

1. BIOTIN 300 MCG 2. D-PANTOTHENIC ACID (CALCIUM D-PANTOTHENATE) 10 MG 3. FOLIC ACID 1 MG 4. NIACINAMIDE 20 MG 5. VITAMIN B1 (THIAMINE MONONITRATE) 1.5 MG 6. VITAMIN B12(CYANOCOBALAMIN) 6 MCG 7. VITAMIN B2 (RIBOFLAVIN) 1.7 MG 8. VITAMIN B6 (PYRIDOXINE HYDROCHLORIDE) 10 MG 9. VITAMIN C (ASCORBIC ACID) 100 MG 10. INERT FILLER (CORNSTARCH)

DIETARY_SUPPLEMENTMedium dose: supplemental zinc, selenium and vitamin E

1. ZINC 50 mg (AS ZINC SULFATE) 2. SELENIUM 75 mcg (AS SODIUM SELENITE) 3. VITAMIN E (D-ALPHA-TOCOPHEROL) (AS SUCCINATE) 250 IU

Sponsors

Alberta Health services
CollaboratorOTHER
Marcello Tonelli
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Stable on hemodialysis for 3 to 36 months 2. Age greater or equal to 18 years 3. Receiving Replavite or equivalent renal vitamin at baseline 4. Receiving 3 dialysis treatments per week

Exclusion criteria

1. Pregnant (sexually active pre-menopausal females must have negative serum pregnancy test at baseline) 2. Pregnancy, kidney transplantation, a dialysis modality switch, or gastrointestinal surgery planned within 6 months 3. Known allergy to corn starch 4. Known allergy to zinc, selenium, vitamin E or renal vitamin. 5. Projected life expectancy of \<6 months 6. Any other conditions or procedures that, in the opinion of the investigator, would impede absorption of the study product. 7. Participants already taking a vitamin E, zinc or selenium supplement (alone or included in another multi-vitamin). 8. Individuals with a history of head or neck cancer in the past 5 years. 9. Ostomy or short gut syndrome. 10. Enroll in another (interventional) trial.

Design outcomes

Primary

MeasureTime frameDescription
Proportion of participants with zinc deficiency90 days following baselineProportion of participants with zinc deficiency in the combined experimental arms compared to the proportion of participants with zinc deficiency in the active comparator arm.

Secondary

MeasureTime frameDescription
Proportion of participants with zinc deficiency180 days following baselineThe proportion of participants with zinc deficiency in each arm compared to each other arm at each time point.
Proportion of participants with selenium deficiency90 days and 180 days following baselineThe proportion of participants with selenium deficiency in each arm compared to each other arm at each time point.
Zinc90 days and 180 days following baselineZinc concentration in each arm compared to each other arm.
Selenium90 days and 180 days following baselineSelenium concentration measured in each arm compared to each other arm.

Other

MeasureTime frameDescription
Proportion of participants with adverse events30 days following last day of interventionThe proportion of participants with adverse events (and by each type of adverse event) in each arm compared to each other arm.
Change in interdialytic weight90 days and 180 days following baselineChange in interdialytic weight in each arm compared to each other arm.
Salt sensitivity90 days and 180 days following baselineThe proportion of participants with recognized and detect salt sensitivities in each arm compared to each other arm.
Proportions of participants with serious adverse events30 days following last day of interventionThe proportion of participants in each arm compared to each other arm experiencing serious adverse events resulting in death, life threatening illness, hospitalization or prolongation of existing hospitalization, or persistent or significant disability.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026