Glycemic Response to Momordica Charantia in Type 2 Diabetes
Type 2 Diabetes

About this trial
This is an interventional treatment trial for Type 2 Diabetes focused on measuring diabetes type 2
Eligibility Criteria
Inclusion Criteria:
- Adult Type 2 diabetics with mild degree of hyperglycemia (FBG >126<200 mg/dl)
- Absence of serious co-morbid conditions
- Patients agreeing to participate in this trial
Exclusion Criteria:
- Type 1 diabetics
- Pregnancy
- Paediatric age group
- Patients known to be allergic to Momordica charantia
- Serious cardio-respiratory illness, previous myocardial infarction, angina pectoris, heart failure, uncontrolled hypertension ≥ stage 2, COPD, asthma, active pulmonary tuberculosis
- Significant hepatic impairment: ALT >60, Bilirubin >2 mg/dl
- Significant renal impairment: S/creatinine >1.5 mg/dl, albuminuria > 1+
- Patients with conditions likely to interfere with the absorption of the trial therapy: malabsorption, chronic diarrhoea, intestinal resection, blind loop syndrome
- Patients withholding consent
- Patients, both male and female, desiring pregnancy during the trial phase.
- Secondary causes of diabetes
- Patients using drugs influencing glucose metabolism: steroids, hormonal contraception, menopausal HRT , diazoxide, phenytoin, colchicine
Sites / Locations
- Services Hospital
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Active Comparator
Placebo
Momordica charantia
placebo powder (wheat flour) The placebo arm will be administered capsules containing a total of 500 mg of starch powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3.
Thirty patients will be assigned to each arm in a double blind manner. The active arm will be administered capsules containing a total of 500 mg of Momordica charantia freeze dried powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3. The placebo arm will be administered capsules containing a total of 500 mg of starch powder, at dose level 1; 1000 mg at dose level 2; 1500 mg at dose level 3.