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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT02414386
Date of registration: 07/04/2015
Prospective Registration: Yes
Primary sponsor: Uniwersytecki Szpital Kliniczny w Opolu
Public title: Serum Vitamin D Levels in Critically Ill Patients Undergoing Regional Citrate Anticoagulation CRRT VitDcrrt
Scientific title: Serum Vitamin D Levels in Multi-organ Failure Critically Ill Patients Undergoing Regional Citrate Anticoagulation Continuous Renal Replacement Therapies - Prospective Observational Case-control Study
Date of first enrolment: August 2015
Target sample size: 40
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02414386
Study type:  Observational
Study design:   
Phase: 
Countries of recruitment
Poland
Contacts
Name:     Tomasz Czarnik, MD PhD
Address: 
Telephone:
Email:
Affiliation:  Department of Anesthesiology and Intensive Care, Uniwersytecki Szpital Kliniczny w Opolu
Key inclusion & exclusion criteria

Inclusion Criteria:

- Respiratory, circulatory failure and acute kidney injury mechanically ventilated
critically ill patients admitted to the critical care unit undergoing regional citrate
anticoagulation continuous renal replacement therapy by means of continuous
veno-venous hemodiafiltration (CVVHDF)

Exclusion Criteria:

- age less than 18 years

- acute liver failure

- hypercalcemia at admission (total calcium plasma level > 10.6 mg/dL; total ionized
calcium plasma level > 1.35 mmol/L)

- parathyroid glands disease at admission

- serum vitamin D level < 10 ng/ml at admission

- end stage renal disease at admission

- lack of relatives consent



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Acute Kidney Injury
Multi Organ Failure
Intervention(s)
Other: biospecimen retention
Primary Outcome(s)
The relationship between vitamin D plasma levels and regional citrate CRRT [Time Frame: 96 hours]
Secondary Outcome(s)
The relationship between other parameters of calcium-phosphate metabolism and regional citrate CRRT [Time Frame: 96 hours]
Secondary ID(s)
VitaminDcitrateCRRT
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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