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Comparison of rise in vitamin D levels after oral dose of vitamin D in obese and non-obese children

Response to single oral dose vitamin D in obese vs non-obese vitamin D deficient children of 5-12 years age

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/04/018640
Enrollment
44
Registered
2019-04-16
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

Health Condition 1: E559- Vitamin D deficiency, unspecified

Interventions

Intervention1: vitamin D: single oral dose of 150,000 IU Vitamin D in obese and non-obese children in age group 5-12 years who are vitamin D deficient Control Intervention1: NIL: NIL

Sponsors

Dr Medha Mittal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Cases- Obese Indian children (Obesity as defined by BMI more than 27 th adult equivalent of Indian Academy of Pediatrics BMI charts) of age group 5 to 12 years presenting to Out-patient clinic and pediatric endocrinology clinic at Chacha Nehru Bal Chikitsalaya, Delhi will be screened and included in the study if their vitamin D levels are less than 20 ng/ml. Controls- Apparently healthy children, not overweight or obese, of age group 5- 12 years presenting to pediatric OPD for minor complaints (like cough, coryza for less than 5 days) will be screened for vitamin D deficiency and included in the study if their vitamin D levels are less than 20 ng/ml.

Exclusion criteria

Exclusion criteria: 1. Children with confirmed or suspected malabsorption, renal or hepatic disorders. 2. Children who have received vitamin D in therapeutic doses in last 6 months. 3. Children on psoralen and ultraviolet A therapy (PUVA) for some skin disorder. 4. Children who have received drugs that may interfere with vitamin D metabolism like anticonvulsants, steroids, chemotherapy, antitubercular drugs, H2 Blockers, and thiazide diuretics and those on any herbal or ayurvedic medications. 5. Children with any known systemic illness or endocrine or metabolic disorder known to be associated with obesity either before or during the course of study or subjects with symptoms suggestive of hypothalamic obesity.

Design outcomes

Primary

MeasureTime frame
Comparison of rise in serum vitamin D levels from baseline at 1-month post supplementation with single 150,000 IU oral dose of vitamin D in obese vs nonobese vitamin D deficient children in age group 5-12 years.Timepoint: Before giving Vitamin D and 1 month post Vitamin D supplementation

Secondary

MeasureTime frame
Hypercalcemia, HypercalciureaTimepoint: 1 week and 1 month after Vitamin D dose

Countries

India

Contacts

Public ContactDr Akshay Tayde

Chacha Nehru Bal Chikitsalaya, Delhi

goelmedha@gmail.com09599718219

Outcome results

None listed

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