Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05657678

Vitamin D3 Supplementation in Critically Ill Patients Undergoing CRRT

Efficacy Comparison of Two Doses of Vitamin D3 in Critically Ill Patients Undergoing Continuous Renal Replacement Therapy

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
138 (estimated)
Sponsor
Uniwersytecki Szpital Kliniczny w Opolu · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Patients hospitalized in intensive care units (ICU) are particularly susceptible to vitamin D3 deficiencies. This can be due to the severity of their underlying disease, the type of treatment they are on, malnutrition before and inadequate nutrition during the hospitalisation preceding ICU admission, as well as advanced age. It has also been established that plasma levels of 25(OH)D3 tend to systematically decrease during ICU treatment. Therapeutic interventions administered in ICU settings such as fluid resuscitation or extracorporeal therapies can cause additional vitamin D3 deficiencies. The incidence of deficiency in critically ill patients can reach up to 90%, and even 30% of ICU patients can have undetectable plasma levels. It is impossible to replenish vitamin D3 levels in critically ill patients with traditional enteral and parenteral nutrition treatment regimens, because nutritional products contain too little of the vitamin. Vitamin D3 deficiency in critically ill patients has been associated with acute kidney injury, acute respiratory failure, sepsis, septic shock and increased all-cause ICU mortality. Despite that, assessment of plasma 25(OH)D3 levels is not a routine practice in ICUs. In view of the prevalence of vitamin D3 deficiencies in ICU patients, rapid replenishment of this deficiency with an increased supplementation dose should be considered as a potential means to improve prognosis in this patient population. The current standard therapy is the administration of 500,000 IU of vitamin D3 via the enteral route in ICU patients with severe deficiency (recommended by ESPEN). The NephroD study is meant to help answer the question whether increasing the standard ICU supplementation dose of vitamin D3 by 50% will ensure a more effective replenishment of this vitamin in critically ill patients undergoing CRRT.

Conditions

Interventions

TypeNameDescription
DRUGVitamin D3 - 750 000 IUa single administration of 750,000 IU of vitamin D3
DRUGVitamin D3 - 500 000 IUa single administration of 500,000 IU of vitamin D3

Timeline

Start date
2022-12-20
Primary completion
2026-01-01
Completion
2026-05-01
First posted
2022-12-20
Last updated
2024-04-23

Locations

4 sites across 1 country: Poland

Source: ClinicalTrials.gov record NCT05657678. Inclusion in this directory is not an endorsement.