CTRI/2017/04/008384已完成4 期
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
Rakesh Ojha0 个研究点目标入组 180 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 180
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Diabetes study:
- •Patients of either gender with known T2DM, aged between 20 and 65 years
- •Patient with borderline blood lipid abnormality and not taking any hypolipidemic agents
- •Patient is on stable monotherapy of Glimeperide 2 mg
- •Patient willing to use Plant based therapy (RESVERATROL) with gold standard therapy in management of their T2DM.
- •Dylipidemia study:
- •Patients with either sex in the age group of 20-65 years suffering from dyslipidemia
- •Patient who are on stable therapy of Atorvastatin 10 mg tablet
- •Patient willing to use Plant based therapy (RESVERATROL) with gold standard therapy (Statin) in management of dyslipidemia.
- •Hypertension study:
- •Patients of either sex, aged 20-65 yrs
- •Patients with Stage I hypertension (SBP 140â??159 mmHg and DBP 90â??99 mmHg)
- •Patients taking monotherapy of Telmisartan 20 mg
- •Patient willing to use Plant based therapy (RESVERATROL) with gold standard therapy (Telmisartan 20 mg) in management of hypertension.
排除标准
- •Diabetes study:
- •Patients who are willing to use other antioxidant supplementation rather than RESVERATROL
- •Patients with type 1 diabetes, pregnant women and lactating mothers
- •Patients with dyslipidemia and taking lipid lowering therapy including statin
- •Patients with history of severe heart disease, hepatic and renal dysfunction
- •Patients taking/requiring beta â?? blocker and any drug which produce hyperglycemia or hypoglycemia.
- •Patients with history of allergy with grapes and consume alcohol daily
- •Dylipidemia study:
- •Patients who are willing to use other antioxidant supplementation rather than RESVERATROL
- •Pregnant women and lactating mothers
- •Patients taking/requiring any drug which affect blood lipid level
- •Patients with history of diabetes, severe heart disease, hepatic and renal dysfunction
- •Patients with history of allergy with grapes and consume alcohol daily
- •Hypertension study:
- •Patients who are willing to use other plant based therapy rather than RESVERATROL
- •Patients taking/requiring any drug which affect blood pressure
- •Pregnant women and lactating mothers
- •Patients with history of severe heart disease, hepatic and renal dysfunction
- •Patients with history of allergy with grapes and consume alcohol daily
研究者
相似试验
进行中(未招募)
1 期
A Study to Evaluate the Efficacy and Safety of Tenofovir Disoproxil Fumarate (TDF) in Combination with Peginterferon alfa-2a (Pegasys) versus Tenofovir Disoproxil Fumarate or Peginterferon alfa-2a Monotherapy for 48 Weeks in Non-Cirrhotic Subjects.EUCTR2010-024586-45-ITGILEAD SCIENCE INC.720
进行中(未招募)
1 期
A Phase 4, Randomized, Open-label, Active-Controlled, Superiority Study to Evaluate the Efficacy and Safety of Tenofovir Disoproxil Fumarate (TDF) in Combination with Peginterferon a-2a (Pegasys®) versus Standard of Care Tenofovir Disoproxil Fumarate Monotherapy or Peginterferon a-2a Monotherapy for 48 Weeks in Non-Cirrhotic Subjects with HBeAg-Positive or HBeAg-Negative Chronic Hepatitis B (CHB).Chronic Hepatitis BMedDRA version: 12.1Level: LLTClassification code 10008910Term: Chronic hepatitis BEUCTR2010-024586-45-FRGilead Sciences Inc.751
进行中(未招募)
4 期
Study to Evaluate the Efficacy and Safety of Tenofovir Disoproxil Fumarate (TDF) in Combination With Peginterferon α-2a vs Standard of Care Tenofovir Disoproxil Fumarate Monotherapy or Peginterferon α-2a Monotherapy for 48 Weeks in Chronic Hepatitis B (CHB).CTRI/2012/11/003083Gilead Sciences Inc720
已完成
4 期
A Phase 4, Randomized, Open-label, Active-Controlled, Superiority Study to Evaluate the Efficacy and Safety of Tenofovir Disoproxil Fumarate (TDF) in Combination with Peginterferon a-2a (Pegasys®) versus Standard of Care Tenofovir Disoproxil Fumarate Monotherapy or Peginterferon a-2a Monotherapy for 48 Weeks in Non-Cirrhotic Subjects with HBeAg-Positive or HBeAg-Negative Chronic Hepatitis B (CHB)HBeAg-Positive or HBeAg-Negative Chronic Hepatitis Binfection of the liver10047438NL-OMON39436Gilead Sciences15
进行中(未招募)
不适用
A study in people with long-lasting hepatitis B to assess the effectiveness and safety of a combination of the two drugs Viread and Pegasys compared with each drug given on its own.EUCTR2010-024586-45-ESGilead Sciences Inc.720
