Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/234494
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dc.date.accessioned2019-03-26T08:51:51Z-
dc.date.available2019-03-26T08:51:51Z-
dc.identifier.urihttp://hdl.handle.net/10603/234494-
dc.description.abstractOBJECTIVES: 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.extentAll Pages
dc.languageEnglish
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dc.rightsuniversity
dc.titleA 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.researcherOjha Rakesh Upendranath
dc.subject.keywordClinical Pharmacy Disease
dc.description.notePharmacology
dc.contributor.guideVyas Bhavin
dc.publisher.placeBarodli
dc.publisher.universityUka Tarsadia University
dc.publisher.institutionFaculty of Pharmacy
dc.date.registered12/7/2013
dc.date.completed2018
dc.date.awarded18/6/2018
dc.format.dimensions
dc.format.accompanyingmaterialCD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Faculty of Pharmacy

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01_title.pdfAttached File228.43 kBAdobe PDFView/Open
02_certificate.pdf664.57 kBAdobe PDFView/Open
03_preliminary.pdf305.56 kBAdobe PDFView/Open
04_chapter 1.pdf215.31 kBAdobe PDFView/Open
05_chapter 2.pdf209.97 kBAdobe PDFView/Open
06_chapter 3.pdf311.65 kBAdobe PDFView/Open
07_chapter 4.pdf330.05 kBAdobe PDFView/Open
08_chapter 5.pdf305.56 kBAdobe PDFView/Open
09_chapter 6.pdf224.17 kBAdobe PDFView/Open
10_chapter 7.pdf196.44 kBAdobe PDFView/Open
11_chapter 8.pdf209.67 kBAdobe PDFView/Open
12_references.pdf247.58 kBAdobe PDFView/Open
13_appendices.pdf14.94 MBAdobe PDFView/Open


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