Health Condition 1: E00-E89- Endocrine, nutritional and metabolic diseases
Conditions
Interventions
Intervention1: response to an increased vs standard dose of oral vitamin d in vitamin d deficient overweight and obese children- an open labelled randomised controlled trial: participants will be rand
Sponsors
none
Eligibility
Inclusion criteria
Inclusion criteria: overweight / obese children of age 5-12 years presenting to the pediatric OPDof cnbc delhi will be screened and included in the study if their serum 25(OH) vitamin D levelks are less than 20ng/ml
Exclusion criteria
Exclusion criteria: 1) children with confirmed or suspected malabsorption, renal or hepatic disorders. 2) children who had received vitamin D in therapeutic doses in the last 6 months. 3) children who had received drugs that may interferev with vitamin D metabolism like anticonvulsants, steriods, chemotherapy, antitubercular, h2 blockers, and thiazide diuretics and those on any herbal or ayurvedic medicines. 4) children with any known systemic illness oer metabolic disroders known to be assiociated with obesity wither before or during study or subjects with sypmtosm s/o hypothalamic obesity like hypothyroidism, cushing syndrome etc.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to evaluate the rise in levels of serum 25(OH)D levels in each group from baseline to 30 days after the last dose of vitamin D.Timepoint: From baseline to 30 days post supplementation of oral Vitamin D . | — |
Secondary
| Measure | Time frame |
|---|---|
| secondary outcome: 1) to measure serum 25(OH)d levels at day 7 2)serum calcium levels post suplementation day 7 & 30 3) urinary calcium creatinine ratio levels post supplementation day 7 and day 30.Timepoint: day 7 & day 30 post supplmentation | — |
Countries
India
Contacts
Public ContactDr.S.Adithya
Chacha Nehru Bal Chikitsalaya
Outcome results
None listed