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http://hdl.handle.net/10603/234494
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DC Field | Value | Language |
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dc.coverage.spatial | ||
dc.date.accessioned | 2019-03-26T08:51:51Z | - |
dc.date.available | 2019-03-26T08:51:51Z | - |
dc.identifier.uri | http://hdl.handle.net/10603/234494 | - |
dc.description.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 | |
dc.format.extent | All Pages | |
dc.language | English | |
dc.relation | ||
dc.rights | university | |
dc.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 | |
dc.title.alternative | ||
dc.creator.researcher | Ojha Rakesh Upendranath | |
dc.subject.keyword | Clinical Pharmacy Disease | |
dc.description.note | Pharmacology | |
dc.contributor.guide | Vyas Bhavin | |
dc.publisher.place | Barodli | |
dc.publisher.university | Uka Tarsadia University | |
dc.publisher.institution | Faculty of Pharmacy | |
dc.date.registered | 12/7/2013 | |
dc.date.completed | 2018 | |
dc.date.awarded | 18/6/2018 | |
dc.format.dimensions | ||
dc.format.accompanyingmaterial | CD | |
dc.source.university | University | |
dc.type.degree | Ph.D. | |
Appears in Departments: | Faculty of Pharmacy |
Files in This Item:
File | Description | Size | Format | |
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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 |
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