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Validation of Prediction Model of Vitamin D Deficiency

Validation of Prediction Model of Vitamin D Deficiency in Critically Ill Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05094388
Enrollment
400
Registered
2021-10-26
Start date
2021-11-10
Completion date
2025-12-31
Last updated
2024-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critical Illness

Keywords

critical care, vitamin D

Brief summary

Many studies have pointed out that patients with vitamin D deficiency have a longer stay in the intensive care unit and a poor prognosis. The investigators' previous multi-center prospective observational study in Taiwan reveals that the prevalence of vitamin D deficiency in critically ill patients in northern Taiwan is 59%, and the prevalence of severe vitamin D deficiency is 18%. The investigators used the data of that observational study to train a predictive model for predicting vitamin D deficiency. In addition, the association between vitamin D and the immune regulation of critically ill patients in Taiwan has not been investigated. This study aims primarily to validate the performance of the prediction model of vitamin D deficiency. Moreover, this study will investigate the association between vitamin D level and inflammatory cytokine levels. This multi-center prospective observational study will enroll critically ill patients admitted to intensive care units (ICUs) less than 28 days. After inform consent, blood will be drawn for examination of vitamin D, interleukin 6, and interleukin 10 levels. The main diagnosis of ICU admission, past medical history, vital signs within 24 hours of admission, disease severity, and laboratory data will be recorded. The predictive model will use the required parameters to predict the patient's risk of vitamin D deficiency and vitamin D severe deficiency.

Interventions

Admitted to intensive care units

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients admitted to intensive care units

Exclusion criteria

* aged \< 20 years * admitted to intensive care unit longer than 28 days * body max index \< 18 kg/m2 * receive vitamin D supplement \> 3000 IU/day * previously admitted to intensive care unit within 3 months * have parathyroid disease, rickets, or severe liver cirrhosis \[Child C\]

Design outcomes

Primary

MeasureTime frameDescription
Area under the receiver operating characteristic1 dayArea under the receiver operating characteristic of the prediction model of vitamin D deficiency

Countries

Taiwan

Contacts

Primary ContactYu-Chang Yeh, MD, PhD
tonyyeh@ntuh.gov.tw+886-9-68661829

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026