Effect of Ayurvedic formulation Vidanga Churna and Vyoshadi Guggulu in the Management of Medoroga (Obesity)
- Conditions
- Health Condition 1: E669- Obesity, unspecified
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
i)Obese subjects of BMI ( >25 to 39.9 kg/m2)
ii)Obese patients of either sex and of age between 18 – 45 years
iii)Willing to participate in the study
i)Obesity due to secondary causes – Hypothyroidism, PCOD,
Cushing’s syndrome etc.
ii)Patients with poorly controlled Hypertension
(BP > 160 / 100 mm Hg)
iii)Patients with uncontrolled Diabetes Mellitus having HbA1C >8%
iv)Patients who are on corticosteroids, Ca++ channel blockers,
Anti-psychotics, antidepressants, anti-cholinergic, anti-epileptics,
immune-suppressants, Hormonal replacement therapy or any
other drugs that may have an influence on outcome of study.
v)Patients with the H/O significant systemic illness which might
interfere with the compliance of the trail drug (Rheumatoid
arthritis, Tuberculosis, Inflammatory Bowel Disease etc.).
vi)Patients who have a past history of Cardiac Arrhythmia,
Acute Coronary Syndrome, Myocardial Infarction, Stroke
or Severe Arrhythmia in the last 6 months.
vii)Symptomatic patients with clinical evidence of congestive
cardiac failure.
viii)Known cases of HIV and AIDS &Patients suffering with malignancy.
ix) Patients with concurrent serious hepatic disorders (defined as
Aspartate Amino Transferase (AST) and / or Alanine Amino
Transferase (ALT) > 2 times upper normal limit) or Renal Disorders
(defined as S. Creatinine >1.2mg/dL), Severe Pulmonary Dysfunction
(uncontrolled Bronchial Asthma and / or Chronic Obstructive
Pulmonary Disease (COPD)
x) Women who are planning for conception / pregnant or lactating.
xi) H/o hypersensitivity to any of the trial drugs or their ingredients.
xii)Any other condition which the Investigator thinks may jeopardize
the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method