Health Condition 1: null- Metabolic syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Male or Female Subjects aged 18-70 years of age Subjects Diagnosed of Metabolic syndrome as per ATPIII criteria Subjects willing to take residential treatment for minimum 21 days
Exclusion criteria
Exclusion criteria: Patients not willing to give consent for the study. H/o CAD, Angina, TMT positive for inducible ischemia. Those suffering from Renal Calculi or had a history of renal calculi in past with oxalate or phytate calculi. Uncontrolled hypertension SBP200mmhg, DBP100 mmhg Uncontrolled diabetes (blood glucose 250mg/dl) with or without diabetic nephropathy or microalbuminuria + ve. Those who are on parental insulin, statins etc. Patients taking other therapies such as homeopathy / ayurveda etc which can have direct or indirect effect on study variables. Abnormal RFT as defined by BUN, S Creatinine 1.2, S Uric acid , Pregnancy / Lactation, Those with Hypothyroidism, Cushing?s syndrome, pheochromocytoma. Intake of steroids / HRT Those who are regularly practicing yoga for last three months Those with Major psychiatric illness with cognitive impairments. Those with known COPD, Congenital heart defects. Those who are on glutamine supplements and protein based nutritional weight loss supplements
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in Framingham cardiac risk score of subjects with metabolic syndromeTimepoint: Baseline and post intervention (day 21) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Fasting Lipid Profile (TC,LDL-C,HDL-C, VLDL, Triglycerides) 2. Systolic and Diastolic Blood pressure 3. Fasting and post prandial blood glucose 4. Anthropometry :Waist Circumference, Hip circumference, W:H ratio, BMI 5. Body composition analysis 6. Serum Insulin 7. CRP 8. Platelet aggregation factor 9. Glutathione peroxides, Glutathione Synthase, glutathione reductase Timepoint: Baseline and post intervention (day 21) | — |
Countries
India