VITamine D Supplementation in RenAL Transplant Recipients - VITALE (VITALE)

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
Laboratoire Crinex
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT01431430
First received: August 22, 2011
Last updated: January 22, 2016
Last verified: January 2016

August 22, 2011
January 22, 2016
January 2012
June 2016   (final data collection date for primary outcome measure)
  • De novo diabetes mellitus [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    De novo diabetes mellitus (fasting glycemia > 7 mmoles/l or glycemia > 11 mmoles/l)
  • Cardiovascular complications [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    Cardiovascular complications (acute coronary heart disease, acute heart failure, lower-extremity arterial disease, cerebrovascular disease).
  • De novo cancer [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    Diagnosis of the incidence of any new cancer
  • Patient death [ Time Frame: 2 years ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01431430 on ClinicalTrials.gov Archive Site
  • Blood pressure control [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    Blood pressure and blood pressure control (number and dosage of antihypertensive drugs)
  • Echocardiography findings [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    Comparison of left ventricular ejection fraction
  • Infection including opportunistic [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    Infection including opportunistic (CMV, pneumocystis, nocardial infection, cryptococcal infection, aspergillosis)
  • Acute rejection episode [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
  • Renal allograft function [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    Renal allograft function including estimated glomerular filtration rate, proteinuria
  • Graft survival [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
  • Phosphocalcic biological and clinical relevant parameters [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    PHOSPHOCALCIC biological and clinical relevant parameters : Evolution of serum 25OHD, calcaemia, phosphataemia, serum PTH, bone mineral density and incidence of fractures
  • Renal lithiasis [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
  • Blood pressure control [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    Blood pressure and blood pressure control (number and dosage of antihypertensive drugs)
  • Echocardiography findings [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    Comparison of left ventricular ejection fraction
  • Infection including opportunistic [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    Infection inclunding opportunistic (CMV, pneumocystis, nocardial infection, crypotococcal infection, aspergillosis)
  • Acute rejection episode [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
  • Renal allograft function [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    Renal allograft function including estimated glomurular filtration rate, proterinuria
  • Graft survival [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
  • Phosphocalcic biological and clinical relevant parameters [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
    PHOSPHOCALCIC biological and clinical relevant parameters : Evolution of serum 25OHD, calcaemia, phosphataemia, serum PTH, bone mineral density and incidence of fractures
  • Renal lithiasis [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
Not Provided
Not Provided
 
VITamine D Supplementation in RenAL Transplant Recipients - VITALE
Prospective Double Blind Multicentre Randomized Trial of Vitamine D Estimating the Profit of a Treatment by Vitamin D3 at the Dose of 100000 UI by Comparison With a Treatment in the Dose of 12 000 UI at Renal Transplanted Patients
It has been proposed that the intake of high dose of cholecalciferol may have beneficial non classical effects (beside bone health). This could include the reduction of type 2 diabetes mellitus, cardiovascular diseases, cancers, autoimmune and infectious diseases. These pleiotropic effects are mostly documented by observational and experimental studies or small intervention trials. In renal transplant recipients, vitamin D insufficiency, defined as circulating 25(OH)vitamin D (25OHD) less than 30 ng/mL, is a frequent finding and this population is at risk of the previously cited complications.The primary purpose of this study is to compare the effects of high dose vs. low dose of cholecalciferol on a composite endpoint consisting in de novo diabetes mellitus, cardiovascular diseases, de novo cancer and patient death.Renal transplant recipients between 12 and 48 months after transplantation will be randomized to blindly receive either high or low dose of cholecalciferol with a follow-up of 2 years.

Rationale :

Vitamin D cannot be considered any more as only necessary to prevent rickets or osteomalacia. Calcitriol produced in the kidney is known to have classical endocrine PHOSPHOCALCIC properties. More recently, vitamin D has been shown to play an important role in reducing the risk of many chronic diseases including type 2 diabetes mellitus, cardiovascular diseases, cancers, autoimmune and infectious diseases. These effects may be secondary to local production of calcitriol and to its autocrine and paracrine actions on cellular proliferation and differentiation, apoptosis, insulin and renin secretion, interleukin and bactericidal proteins production. These pleiotropic effects are mostly documented by observational and experimental studies or small intervention trials that most often evaluated intermediate parameters. In renal transplant recipients, vitamin D insufficiency (circulating 25OHD<30 ng/mL or 75 nmol/L) , is a frequent finding with more than 80% of patients displaying this profile.

Objective:

Primary objective: compare the effects of high dose vs. low dose of cholecalciferol on a composite endpoint including

  • De novo diabetes mellitus (fasting glycemia > 7 MMOLES/l or glycemia > 11 MMOLES/l)
  • Cardiovascular complications (acute coronary heart disease, acute heart failure, lower-extremity arterial disease, cerebrovascular disease).
  • De novo cancer,
  • Patient death.

Secondary objectives : compare the effects of high dose vs. low dose of cholecalciferol on

  • The occurrence of each event constituting the primary endpoint
  • Blood pressure and blood pressure control (number and dosage of antihypertensive drugs)
  • Echocardiography findings
  • Infection including opportunistic (CMV, pneumocystis, nocardial infection, cryptococcal infection, aspergillosis)
  • Acute rejection episode
  • Renal allograft function including estimated glomerular filtration rate and proteinuria - Graft survival
  • PHOSPHOCALCIC biological and clinical relevant parameters : Evolution of serum 25OHD, calcaemia, phosphataemia, serum PTH, bone mineral density and incidence of fractures
  • Renal lithiasis

Study protocol

Number of patients: 320 patients in each group Inclusions : 2 years Follow-up after inclusion : 2 years Prospective, randomized, multicentre, double blind clinical study comparing high dose cholecalciferol [100 000 UI FORTHIGHTLY for 2 months then monthly for 22 months) vs. low dose cholecalciferol [12 000 UI FORTHIGHTLY for 2 months then monthly for 22 months).

Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Renal Transplant Candidate for Right Kidney
  • Drug: Cholecalciferol 100 000 UI
    Cholecalciferol 100 000 UI FORTHIGHTLY for 2 months then monthly for 22 months
  • Drug: Cholecalciferol 12 000 UI
    Cholecalciferol 12 000 UI FORTHIGHTLY for 2 months then monthly for 22 months.
  • Experimental: Cholecalciferol 100 000 UI
    Cholecalciferol 100 000 UI FORTHIGHTLY for 2 months then monthly for 22 months
    Intervention: Drug: Cholecalciferol 100 000 UI
  • Active Comparator: Cholecalciferol 12 000 UI (Control)
    Cholecalciferol 12 000 UI FORTHIGHTLY for 2 months then monthly for 22 months.
    Intervention: Drug: Cholecalciferol 12 000 UI
Courbebaisse M, Alberti C, Colas S, Prié D, Souberbielle JC, Treluyer JM, Thervet E. VITamin D supplementation in renAL transplant recipients (VITALE): a prospective, multicentre, double-blind, randomized trial of vitamin D estimating the benefit and safety of vitamin D3 treatment at a dose of 100,000 UI compared with a dose of 12,000 UI in renal transplant recipients: study protocol for a double-blind, randomized, controlled trial. Trials. 2014 Nov 6;15:430. doi: 10.1186/1745-6215-15-430.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
538
December 2016
June 2016   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Renal transplant recipients between 12 and 48 months after transplantation with a stable renal function during the past 3 months.
  • Vitamine D insufficiency defined as a concentration of 25OHD lower than 30 ng/ml.
  • Patient between 18 and 75 years old
  • Patient capable of understanding the advantages and the risks of the study.
  • Affiliated with social security health insurance
  • Written informed consent

Exclusion Criteria:

  • Calcaemia > 2,7 mmol/l
  • Phosphataemia > 1,5 mmol/l
  • Serum creatinine > 250 µmol/l
  • Treatment by an active form of the vitamin D not being able to be interrupted
  • Transplant of an organ other than the kidney
  • Type I or type II diabetes mellitus
  • Past medical history of granulomatosis or active granulomatosis
  • Primary hyperoxaluria
  • Malabsorption proved by the liposoluble vitamins
  • Simultaneous participation in another therapeutic essay
  • Patients presenting a drug addiction or a psychiatric disorder
  • Pregnant or breast-feeding women
  • Vitamin D hyper sensibility
Both
18 Years to 75 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT01431430
P100103
Yes
Not Provided
Not Provided
Assistance Publique - Hôpitaux de Paris
Assistance Publique - Hôpitaux de Paris
Laboratoire Crinex
Principal Investigator: Eric THERVET, MD, PhD European Georges Pompidou Hospital
Assistance Publique - Hôpitaux de Paris
January 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP