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The efficacy and safety of daily oral vitamin D2 in the treatment of vitamin D deficiency in adults(VD2-2022)

The efficacy and safety of daily oral vitamin D2 in the treatment of vitamin D deficiency in adults(VD2-2022)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079573
Enrollment
Unknown
Registered
2024-01-06
Start date
2024-01-06
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Vitamin D deficiency

Interventions

25(OH)D < 10 ng/mL and daily oral supplementation of vitamin D2 group:Daily oral supplementation of 5000 units vitamin D2
25(OH)D < 10 ng/mL and oral supplementation of vitamin D2 every other day group:Oral supplementation of 5000 units vitamin D2 every other day
25(OH)D<10 ng/mL and daily oral supplementation of vitamin D3 group:Daily oral supplementation of 800 units vitamin D3
25(OH)D = 10 ng/mL and daily oral supplementation of vitamin D2 group:Daily oral supplementation of 5000 units vitamin D2 group
25(OH)D = 10 ng/mL and oral supplementation of vitamin D2 every other day group:Oral supplementation of 5000 units vitamin D2 every other day
25(OH)D = 10 ng/mL and daily oral supplementation of vitamin D3 group:Daily oral supplementation of 800 units vitamin D3

Sponsors

The Second Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. 25-hydroxyvitamin D level < 20 ng/ml; 2. Aged between 18 and 60 years; 3. No liver or kidney dysfunction or other serious diseases; 4. No long-term travel planned in the tropical region within 12 months after the trial started; 5. Willingness to participate in this study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Vitamin D supplements in the last 6 months; 2. A history of any drugs that could affect vitamin D metabolism in the last 6 months; 3. Reluctance to participate in research; 4. A history of cognitive impairment or somatic dysfunction affecting completion of study; 5. A history of Hypercalcemia, vitamin D overdose or poisoning, renal insufficiency, chronic diarrhea, hypoproteinemia, or other conditions affecting vitamin D metabolism.

Design outcomes

Primary

MeasureTime frame
25-hydroxyvitamin D3;25-hydroxyvitamin D2;25-hydroxyvitamin D;

Secondary

MeasureTime frame
Serum calcium;Serum creatinine;24-hour urine calcium;24-hour urine creatinine;Liver function;Serum osteocalcin;Serum intact parathyroid hormone;Serum ß-C-terminaltelopeptide typeIcollagen;Serum N-terminal propeptide of type I procollagen;Body composition;Grip strength;Vitamin D binding protein;

Countries

China

Contacts

Public ContactZhongjian Xie

The Second Xiangya Hospital, Central South University

zhongjian.xie@csu.edu.cn+86 173 0847 9573

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026