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Vitamin D Supplementation in Intensive Care Unit Patients

Phase 3
Completed
Conditions
Intensive Care Unit
Vitamin D Toxicity
Vitamin D Deficiency
Dietary Supplements
Interventions
Dietary Supplement: Vitamin D supplementation
Registration Number
NCT04915963
Lead Sponsor
Association Tunisienne d'Etude & de Recherche sur l'Athérosclérose
Brief Summary

A randomized controlled trial is designed to investigate the safety and clinical efficacy of a mega dose of VD in patients admitted in intensive care unit (ICU). Patients will be randomly allocated to receive 400,000 IU of VD3 or placebo. They will be followed up until ICU discharge or death or the 15th day of ICU stay. Adverse events that occur during ICU stay is collected. Primary outcome is intensive care unit-acquired infection (ICU-AI), and secondary outcomes are septic shock, organ failure, and ICU-mortality. Plasma 25-hydroxyvitamin D is assessed at baseline and at the end of follow-up. Cox regression models will be applied to test how VD supplementation affects adverse outcomes while adjusting for confounders.

Detailed Description

The randomized controlled trial aimed to investigate the safety and clinical efficacy of a single mega dose of vitamin D (VD) in patients admitted at intensive care unit (ICU).

Study participants: VD deficient ICU patients

Criteria of inclusion, patients:

* newly admitted (within 24 hours)

* over eighteen,

* able to receive medication orally or through nasogastric tube

* expected to stay more than 72 hours in ICU.

Criteria for non-inclusion and exclusion, patients:

* lack of patient's or relatives' consent

* expected short life or ICU stay (\<48 hours)

* sepsis at admission

* kidney, liver or intestinal disease

* hypercalcemia (total calcium\>10.6 mg/dL)

* history of a disorder associated with hypercalcemia (cancer, tuberculosis, sarcoidosis, hyperparathyroidism, nephrolithiasis)

* treatment with immunotherapy or vitamin supplements within one year

* pregnant or breastfeeding women

* discharge from ICU or death within 72 hours of admission

Study protocol

Patients will undergo physical examination with calculation of acute physiology and chronic assessment II (APACHE II) and sequential organ failure assessment (SOFA) scores. They will be randomly assigned to either VD or placebo group after stratification on gender, age and APACHE II:

* VD group, 170 patients will receive a single dose of 400,000 IU of VD3 orally or through nasogastric tube

* Placebo group, 170 patients will receive distilled water orally or through nasogastric tube.

The patients will followed up until ICU discharge or death or the 15th day of ICU stay, whichever occurs first and adverse events that occurred during ICU stay were collected.

Primary outcome: intensive care unit-acquired infection (ICU-AI), defined as an infection of blood stream, lower respiratory tract, urinary tract, skin/soft tissue or gastrointestinal tract, which was not present within the first 48 hours of admission into the ICU.

Secondary outcomes: urinary calcium:creatinine ratio as surrogate for VD toxicity, septic shock, organ failure, ICU-mortality.

Plasma 25-hydroxyvitamin D (25-OHD) will be assessed at baseline and the end of follow-up using immunoassay.

Cox regression models will be applied to test how VD supplementation affects adverse events and ICU-mortality while adjusting for confounders.

Hypothesis. Recovering an adequate VD status might reduce poor outcome, especially infectious outcomes in ICU patients.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
340
Inclusion Criteria
  • newly admitted (within 24 hours)
  • over eighteen,
  • able to receive medication orally or through nasogastric tube
  • expected to stay more than 72 hours in ICU
  • given consent
Exclusion Criteria
  • lack of patient's or relatives' consent
  • expected short life or ICU stay (<48 hours)
  • sepsis at admission
  • kidney, liver or intestinal disease
  • hypercalcemia (total calcium>10.6 mg/dL)
  • history of a disorder associated with hypercalcemia (i.e., cancer, tuberculosis, sarcoidosis, hyperparathyroidism, nephrolithiasis)
  • treatment with immunotherapy or vitamin supplements within one year
  • pregnant or breastfeeding women
  • discharge from ICU or death within 72 hours of admission

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Placebo groupVitamin D supplementation170 patients receiving distilled water (2 vials of 1 ml distilled water) orally or through a nasogastric tube
vitamin D groupVitamin D supplementation170 patients receiving a single dose of 400,000 IU of VD3 (2 vials of 200,000 IU VD3; B.O.N., BOUCHARA RECORDATI) orally or through a nasogastric tube
Primary Outcome Measures
NameTimeMethod
Rate of intensive care unit-acquired infection (ICU-AI)15 days

Infection of blood stream, lower respiratory tract, urinary tract, skin/soft tissue or gastrointestinal tract, which was not present within the first 48 hours of admission into the ICU, which occur during the ICU stay.

Secondary Outcome Measures
NameTimeMethod
urinary calcium:creatinine ratio15 days

used as a surrogate for VD toxicity

Rate of septic shock15 days

persisting hypotension requiring vasopressors to maintain a mean arterial pressure of\<65 mm Hg and a serum lactate level \>2 mmol/L despite adequate volume resuscitation .

Rate of organ failure15 days

acute change in sequential organ failure assessment (SOFA) score of 2 points or greater secondary to infection

Rate of ICU-mortality15 days

Death within the ICU

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