Vitamin d trial aims to shield kidneys in critical illness
NCT ID NCT02962102
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether giving activated vitamin D (calcifediol and calcitriol) to critically ill patients in the ICU could prevent or lessen acute kidney injury (AKI). Researchers enrolled 150 adults at high risk for AKI. The goal was to see if this treatment could reduce deaths, the need for dialysis, and kidney damage.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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150 people
The number who actually took part.
- Started
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Apr 2017
- Finished
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Aug 2020
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 * Admitted to the ICU within 48h prior to enrollment * Likely to remain in the ICU (alive) for ≥72h * Naso/orogastric tube or ability to swallow * High risk of severe AKI Exclusion Criteria: * Serum total calcium \> 9.0 mg/dl or phosphate \> 6.0 mg/dL within previous 48h * Currently receiving oral calcium supplementation * Ingestion of vitamin D3 \>1,000 IU/day or any 25-hydroxyvitamin D or 1,25-dihydroxyvitamin D during the previous 7 days * AKI stage 2 or 3 (based on KDIGO serum creatinine and/or urine output criteria) * History of transplantation or receiving chronic (\>7days) of immunosuppressive medications (not including glucocorticoid steroids at a dose less than or equivalent to prednisone 20 mg/day) * Neutropenia in the previous 48h * Active primary parathyroid disease, active granulomatous disease, or symptomatic nephrolithiasis in the previous 3 months * Receiving cytochrome P450 inhibitors * Chronic Kidney Disease stage V or End Stage Renal Disease * Hemoglobin \< 7 g/dL * GI malabsorption * Prisoner * Pregnancy or breast feeding
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
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Other studies related to the condition(s) this trial covers.
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