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Clinical Trials/NCT04262934
NCT04262934
Unknown
Phase 3

Multicenter Randomized Study : Does Correction of 25 OH-VITAmin D With Cholecalciferol Supplementation Increase Muscle Strength in hemoDIALysis Patients?

Institut Phoceen de Nephrologie1 site in 1 country150 target enrollmentJanuary 8, 2018

Overview

Phase
Phase 3
Intervention
Cholecalciferol 100.000 UI administration
Conditions
hemoDIALysis Patients
Sponsor
Institut Phoceen de Nephrologie
Enrollment
150
Locations
1
Primary Endpoint
Muscle strength evaluation after 6 months period after cholecalciferol or no vitamin D treatment
Last Updated
3 years ago

Overview

Brief Summary

Muscle strength decreases as renal failure progresses. Low muscle strength affects more than 50% of hemodialysis patients and leads to daily life activities impairment. In the general population, numerous studies have linked low 25OH-vitamin D (25OHD) concentrations to the loss of the muscle strength and low physical performances. Data on native vitamin D and muscle function are scarce in the chronic renal failure (CKD) population, but low 25OHD levels have been associated with poor muscle strength. In this protocol of an ongoing study named VITADIAL testing if cholecalciferol supplementation in hemodialysis patients with low 25OHD improve their muscle strength.

Detailed Description

Prospective open randomized French multicenter study. All patients will have 25OHD levels ≤50nmol/L at randomization. One group will receive 100 000 UI cholecalciferol once a month during 6 months, the other group will receive no treatment during 6 months. In order to randomize patients with 25OHD ≤50nmol/L, supplemented patients will undergo a 3 months wash-out period renewable 3 times (maximum of 12 months wash-out) until 25OHD reaches a level≤50nmol/L. The main objective of this study is to analyze if a 6 months period of oral cholecalciferol (i.e. native vitamin D) supplementation improves muscle strength of hemodialysis patients with low 25OHD vitamin D levels. Muscle strength will be assessed at 0, 3 and 6 months, by handgrip strength measured with a quantitative dynamometer. Secondary objectives are 1) to analyze 25OHD plasma levels after vitamin D wash-out and/or supplementation, as well as factors associated with 25OHD lowering speed during wash-out and 2) to analyze if this supplementation improves patient's autonomy, reduces frailty risk and improves quality of life.

Registry
clinicaltrials.gov
Start Date
January 8, 2018
End Date
June 8, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • under hemodialysis for more than 3 months
  • aged over 18 years-old
  • gave their consent
  • Non-inclusion criteria :
  • non fluent French speaker
  • incapacity to provide consent or to answer questionnaires
  • pregnancy or breast feeding
  • cognitive impairment
  • bedridden or life expectancy \<1 year
  • active cancer

Exclusion Criteria

  • 25OHD\>50nmol/L after 12 months wash-out
  • hypercalcemia \>2.7mmol/L
  • hyperparathyroidism (iPTH\>9x normal laboratory maximal value) during wash-out or after randomization if patient is in the no treatment group
  • hypoparathyroidism (iPTH\<3x normal laboratory lower value) in a patient receiving cholecalciferol
  • cholecalciferol intolerance or allergy
  • death, renal transplantation
  • pregnancy
  • consent withdrawal
  • renal recuperation allowing hemodialysis to stop
  • unability to perform handgrip

Arms & Interventions

Cholecalciferol treatment

Arm A : Cholecalciferol 100.000 UI - oral - every month

Intervention: Cholecalciferol 100.000 UI administration

No treatment

Arm B : No vitamin D administration

Intervention: No vitamin D administration

Outcomes

Primary Outcomes

Muscle strength evaluation after 6 months period after cholecalciferol or no vitamin D treatment

Time Frame: At 6 months after randomization

Muscle strength will be assessed by handgrip strength measured with a quantitative dynamometer

Secondary Outcomes

  • Patient's autonomy after 6 months period of oral cholecalciferol(At 6 months post randomization (for patients treated))
  • Patient's frailty risk after 6 months period of oral cholecalciferol(At 6 months post randomization (for patients treated))
  • Patient's quality of life after 6 months period of oral cholecalciferol(At 6 months post randomization (for patients treated))

Study Sites (1)

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