Health Condition 1: E559- Vitamin D deficiency, unspecified
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age group 30 to 49 years and BMI = 27 Kg/m2 having = 1 full term delivery Confirmed radiological diagnosis of NAFLD Vitamin D level Individual willing to undergo study and follow all procedures
Exclusion criteria
Exclusion criteria: Known cases of T2DM Individuals with known history of any other endocrinological disorders like Hypothyroidism, PCOS etc. Pregnant or lactating females
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the efficacy of theraputic diet in hypovitaminosis D in obese females with NAFLD. Once recruited, all participants will undergo blood investigations viz. lipid profile (cholesterol, triglycerides, LDL & HDL), fasting blood glucose & insulin, adipokines (adiponectin & leptin). Efficacy will be assessed by difference in values of the above-mentioned lab investigations pre and post study and conclusions derived from appropriate statistical analysisTimepoint: Baseline, 4 weeks, 8 weeks, 12 weeks, 16 weeks, 20 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) 1)To study the association between adipose tissue dysfunction and bioavailability and absorption of vitamin D. 2) To assess association between NAFLD, and hypovitaminosis D.Timepoint: Baseline, 4 weeks, 8 weeks, 12 weeks, 16 weeks, 20 weeks and post-study follow up at 24 weeks | — |
Countries
India
Contacts
Bharati Vidyapeeth (Demeed to be University) College of Ayurved and Hospital