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Effect of Vitamin D3 Supplementation on Serum Interleukin-6 and Hepcidin Levels in Children with Chronic Kidney Disease

Effect of Vitamin D3 Supplementation on Serum Interleukin-6 and Hepcidin Levels in Children with Chronic Kidney Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20250915010
Enrollment
30
Registered
2025-09-15
Start date
2024-09-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

children with CKD Vitamin D3 Hepcidin Interleukin-6 Chronic Kidney Disease Children

Interventions

GFR greater than or equal to 90 mL per min per 1.73 m,GFR less than 90 mL per min per 1.73 m
Screening,Screening

Sponsors

Self-funding
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1. Children aged 2 to 18 years. 2. Diagnosed with chronic kidney disease (CKD). 3. Recruited from the pediatric nephrology inpatient and outpatient wards at our Inst

Exclusion criteria

Exclusion criteria: Exclusion Criteria: 1. Children with malignancy. 2. Children who have received a blood transfusion within the past 3 months. 3. Children with a history of bleeding within the past 3 months. 4. Children with liver dysfunction. 5. Children currently experiencing an infectious disease. 6. Children who have previously or are currently consuming vitamin D3 supplements.

Design outcomes

Primary

MeasureTime frame
Vitamin D, Hepcidin, and Interleukin-6 levels All participants underwent examinations for urea, creatinine, serum vitamin D, hepcidin, and IL-6 levels both before and after vitamin D3 supplementation at a dose of 2,000 IU per day for 6 weeks ng/mL

Secondary

MeasureTime frame
Characteristic data, Characteristic data is to be recorded after vitamin D3 supplementation at a dose of 2,000 IU per day for 6 weeks. age, sex, ,Nutritional status, Comorbid Nutritional status and comorbid data is to be recorded after vitamin D3 supplementation at a dose of 2,000 IU per day for 6 weeks. Underweight, Normal weight, and Overweight

Countries

Indonesia

Contacts

Public ContactNicholas Redly

Department of Pediatrics, Faculty of Medicine, Hasanuddin University, Makassar, Indonesia

nredly021@gmail.com62411855707

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026