Type 2 Diabetes Mellitus
Conditions
Keywords
FBS,HbA1C, PPBS
Brief summary
This study is an open label, two armed trial evaluating the safety and efficacy of Fenfuro capsule twice daily for 90 days in 100 patients with type 2 diabetes that will be conducted in single center in India. The primary outcome measures will be the determination of decrease in plasma glucose levels from baseline to last visit. The secondary outcome will be the determination of safety of Fenfuro capsule in type 2 diabetic subjects.
Detailed description
Diabetes mellitus, involving rise in blood sugar levels, has shown to be a highly prevalent disease. Treatments and treatment regimens include combinations of oral anti-diabetic drugs (OADs), anti-hypertensive medications and anti-dyslipidemic agents, but these have been less than successful in managing their respective disease targets with clinical goals. Now-a-days, the treatment strategies for diabetes mellitus type 2 which are opted by general population include natural supplements. This choice is based upon the involvement of very less side effects along with high effectiveness of the natural supplements as compared to the synthetic medications. One of those natural supplements is fenugreek seeds extract i.e. Fenfuro which has been used as a nutraceutical in the present study for the management of type 2 diabetes mellitus. Fenugreek has been extensively used as a source of anti-diabetic compounds from long time. Thus, Fenfuro, prepared from fenugreek seeds extract, is supposed to have anti-diabetic properties as well. Previous studies on fenugreek seeds extract have shown effective and safe anti-diabetic and anti-hyperlipidemic properties of it. It has shown to decrease blood glucose levels as well as lipid profile of the diabetic patients. In this proposed study, Fenugreek seed extract will be used as an add-on to the existing therapy in patients with type-2 diabetes. The efficacy and safety of the extract will be evaluated using standard methodology.
Interventions
DRUGFenfuro
Sponsors
Chemical Resources
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Agrees to written as well as audio-visual informed consent. * Patients of either sex. * Aged 18-65 years. * Fasting plasma glucose level \<180 mg/dL. * HbA1c level more than 7.5%. * Not receiving any steroids. * Patient on anti-diabetic therapy.
Exclusion criteria
* Uncooperative Subjects. * Diabetes other than type-2 diabetes mellitus. * Evidence of renal & liver disease. * History of any hemoglobinopathy that may affect determination of HbA1c. * Lactating and Pregnant or planning to conceive females. * Physically/ mentally unwell as certified by physician-in-charge. * Participation in any other clinical trial with in the last 30 days. * Subjects with allergy to investigational product.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in Fasting Blood Sugar | On completion of treatment (i.e.12 weeks) as compared to baseline |
| Change in Postprandial sugar | On completion of treatment (i.e.12 weeks) as compared to baseline |
Secondary
| Measure | Time frame |
|---|---|
| Change in HbA1c levels | On completion of treatment (i.e.12 weeks) as compared to baseline |
| SGPT,SGOT,ALP,Creatinine,TLC,DLC & Hb | On completion of treatment (i.e.12 weeks) as compared to baseline |
Countries
India
Outcome results
None listed