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To study the gender-wise difference in Vit B12 and Vit D deficiency, Gender wise categorization of clinical symptoms and reversal of symptoms with appropriate supplementation with vitamin B12 or vitamin D pills

â?? Vitamin B12 and Vitamin D deficiency gender-wise categorization of clinical symptoms and reversal of symptoms with appropriate supplementation-A RCT.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034312
Enrollment
80
Registered
2021-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Nil: Nil Intervention2: Vitamin B12: One tablet of Vitamin B12 per day for four weeks Control Intervention1: Vitamin B12 and Vitamin D: One tablet of Vitamin B12 and Vitamin D per day f

Sponsors

Deenanath Mangeshkar Hospital and Research Center Pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Normal plasma Vitamin B12 and Vitamin D levels 2. Plasma Vitamin B12 30 ng/dL 3. Plasma Vitamin B12 <250 pg/ml and vitamin D < 30 ng/dL

Exclusion criteria

Exclusion criteria: 1.Subjects taking B12 supplementation 2. Subjects on medication which interferes with B12 absorption and metabolism (e.g. methorexate, anta cids, metformin) 3. Subjects with diabetes, cancer, pregnancy., known chronic systemic diseases. 4. Age-below18 years

Design outcomes

Primary

MeasureTime frame
Gender wise differentiation of clinical symptoms and post supplementation reversal of vitamin B12 and Vitamin D deficiencyTimepoint: 6 months

Secondary

MeasureTime frame
Improvement of vitamin B12 and D status with supplementationTimepoint: 6 months

Countries

India

Contacts

Public ContactDr Sadanand S Naik

Deenanath Mangeshkar Hospital and Res centre Pune

dr.sadanandnaik@gmail.com02049153178

Outcome results

None listed

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