Please use this identifier to cite or link to this item:
http://hdl.handle.net/10603/234494
Title: | A Randomized Open Label Active Control Phase IV Clinical Study Evaluating Efficacy and Safety of Resveratrol As an Adjuvant Therapy in Patients with Diabetes Dyslipidemia and Hypertension |
Researcher: | Ojha Rakesh Upendranath |
Guide(s): | Vyas Bhavin |
Keywords: | Clinical Pharmacy Disease |
University: | Uka Tarsadia University |
Completed Date: | 2018 |
Abstract: | OBJECTIVES: The aim of this study was to investigate the efficacy and safety of resveratrol as an adjuvant therapy in newly diagnosed type 2 diabetes mellitus (T2DM) patients with borderline dyslipidemia (Diabetes study), in newly diagnosed dyslipidaemia patients (dyslipidemia study) and newly diagnosed hypertensive patients (hypertension study). newlineSUBJECTS AND METHODS: In this randomized active-controlled study, T2DM patients (male/female) aged 20-65 years with borderline dyslipidemia (hypolipidemic naïve patients) were randomized to receive glimepiride 2mg or glimepiride 2mg plus resveratrol 1 gram daily for 12 months (for Diabetes study). In dyslipidemia study, dyslipidaemia patients (male/female) aged 20-65 years were randomized to receive (1:1) either atorvastatin (10 mg daily) or atorvastatin (10 mg daily) plus resveratrol (500mg twice daily) as adjuvant therapy for 12 months. In hypertension study, patients with Stage I hypertension (SBP 140 159 mmHg and DBP 90 99 mmHg)) were randomized to receive telmisartan 20 mg or telmisartan 20 mg plus resveratrol 1 gram daily for 12 months. In Diabetes study, change in plasma blood glucose (fasting and postprandial); glycosylated hemoglobin (HbA1c); and lipid profile (total cholesterol [TC], Triglycerides [TG], low-density lipoprotein [LDL] and high-density lipoprotein [HDL]) from baseline was assessed. In dyslipidemia study, change in lipid profile (total cholesterol [TC], Triglycerides [TG], low-density lipoprotein [LDL] and high-density lipoprotein [HDL]) from baseline was assessed. In hypertension study, change in systolic blood pressure and diastolic blood pressure from baseline was assessed. Efficacy variable was measured at every 3 months for 12 months for Diabetes, dyslipidaemia and hypertension study. Treatment-emergent adverse events (TEAEs) were assessed at every 3 months for 12 months for Diabetes, dyslipidaemia and hypertension study. newline newline |
Pagination: | All Pages |
URI: | http://hdl.handle.net/10603/234494 |
Appears in Departments: | Faculty of Pharmacy |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
01_title.pdf | Attached File | 228.43 kB | Adobe PDF | View/Open |
02_certificate.pdf | 664.57 kB | Adobe PDF | View/Open | |
03_preliminary.pdf | 305.56 kB | Adobe PDF | View/Open | |
04_chapter 1.pdf | 215.31 kB | Adobe PDF | View/Open | |
05_chapter 2.pdf | 209.97 kB | Adobe PDF | View/Open | |
06_chapter 3.pdf | 311.65 kB | Adobe PDF | View/Open | |
07_chapter 4.pdf | 330.05 kB | Adobe PDF | View/Open | |
08_chapter 5.pdf | 305.56 kB | Adobe PDF | View/Open | |
09_chapter 6.pdf | 224.17 kB | Adobe PDF | View/Open | |
10_chapter 7.pdf | 196.44 kB | Adobe PDF | View/Open | |
11_chapter 8.pdf | 209.67 kB | Adobe PDF | View/Open | |
12_references.pdf | 247.58 kB | Adobe PDF | View/Open | |
13_appendices.pdf | 14.94 MB | Adobe PDF | View/Open |
Items in Shodhganga are licensed under Creative Commons Licence Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0).
Altmetric Badge: