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Vitamin D3 Substitution in Vitamin D Deficient Kidney Transplant Recipients

VITA-D: Cholecalciferol Substitution in Vitamin D Deficient Kidney Transplant Recipients: A Randomized, Placebo-controlled Study to Evaluate the Posttransplant Outcome

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00752401
Acronym
VITA-D
Enrollment
200
Registered
2008-09-15
Start date
2009-05-31
Completion date
2014-07-31
Last updated
2014-01-22

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

Conditions

Kidney Transplantation, Renal Osteodystrophy, Vitamin D Deficiency

Keywords

Vitamin D, Cholecalciferol, Vitamin D3, 25-hydroxyvitamin D3, Immunomodulation, Vitamin D deficiency, Kidney transplantation, Renal transplantation, Graft function, Acute rejection, Renal osteodystrophy, Posttransplant bone loss

Brief summary

The purpose of the study is to evaluate the effects of Cholecalciferol (Vitamin D3) substitution on the posttransplant outcome (glomerular filtration rate as well as serum creatinine levels, number of acute rejection episodes, number of infections and C-reactive protein levels within the first year after transplantation) in vitamin D deficient kidney transplant recipients.

Detailed description

Apart from its classical actions in calcium homeostasis, vitamin D acts as a potent immunomodulatory agent. As such, vitamin D is thought to have beneficial effects in the transplant setting, especially in kidney transplant recipients considering the fact that approximately 40% of all kidney transplant recipients are vitamin D deficient. Therefore, the objective is to conduct a randomized, double-blind, placebo-controlled study focusing on the impact of Cholecalciferol substitution in vitamin D deficient kidney transplant recipients on graft function (glomerular filtration rate as well as serum creatinine levels), incidence of acute rejection episodes, frequency and severity (CRP levels) of posttransplant infections within the first year after kidney transplantation. Moreover, the impact of Vitamin D3 on renal osteodystrophy will be analyzed by means of bone mineral density. DXA measurements will be performed during the first four weeks after kidney transplantation, after 5, and after 12 months posttransplant. Kidney transplant recipients found to have vitamin D deficiency (defined as 25-hydroxyvitamin D \< 50 nmol/l) will be included and will be randomized to receive either oral Vitamin D3 therapy or placebo. Vitamin D3 will be administered at a daily dose of 6800IU over a time period of one year. All in all, 200 subjects will be included in the VITA-D study.

Interventions

DRUGCholecalciferol

6800 IU of Cholecalciferol will be administered in the form of Oleovit® D3-drops once a day for one year. Treatment starts on day 5 after kidney transplantation. At serum calcium levels \>2,65 mmol/l vitamin D3 administration will be reduced to 3600 IU per day. If calcium levels persist above 2,85 mmol/l over a period of four weeks vitamin D3 administration will be discontinued and restarted when serum calcium levels declined to ≤ 2,65 mmol/l with only 3600 International Units per day.

DRUGPlacebo

An oral placebo solution matching Cholecalciferol in terms of appearance, smell and taste will be administered once a day for one year. Treatment starts on day 5 after kidney transplantation.

Sponsors

Medical University of Vienna
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 85 Years
Healthy volunteers
No

Inclusion criteria

* age \> 18 * deceased donor kidney transplant recipients * only kidney transplant recipients * vitamin D deficiency defined as 25 (OH)D \< 50nmol/l

Exclusion criteria

* re-transplantation for the second time if the patient is highly immunized and therefore included in the aphaeresis program * re-transplantation for the third or further time * significant impaired intestinal resorption: malabsorption due to celiac sprue, systemic scleroderma; maldigestion due to chronic pancreatitis, pancreatic insufficiency, pancreas resection, mucoviscidosis, Zollinger-Ellison-syndrome * history of inflammatory bowel disease: Crohn's disease, ulcerative colitis * previous gastrectomy, small bowel or large bowel resection, intestinal bypass surgery * severe liver disease: cirrhosis * HIV positive

Design outcomes

Primary

MeasureTime frame
The immunologic effects of Vitamin D3 substitution in vitamin D deficient kidney transplant recipients will be evaluated by means of: Glomerular filtration rateone year after kidney transplantation
Number of acute rejection episodesone year after kidney transplantation
Number of infectionsone year after kidney transplantation
CRP levelsone year after kidney transplantation
Courses of calcium levelswithin the first year after kidney transplantation

Secondary

MeasureTime frame
The impact of Vitamin D3 substitution on renal osteopathy will be analyzed by means of absolute bone mineral density (g/cm2)within the first year after kidney transplantation

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026