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临床试验/CTRI/2012/02/002463
CTRI/2012/02/002463已完成未知

AN OPEN LABELLED EFFICACY AND TOLERABILITY STUDY OF NOVEL BETA-1- BLOCKER , NEBIVOLOL, ON HYPERTENSION WITH SPECIAL REFERENCE TO ENDOTHELIAL FUNCTION AND ARTERIAL STIFFNESS.

izams Institute of Medical Sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
50

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

  • ) Ambulatory, Male and Female Volunteers between 18-55 years of age with a Body Mass Index (BMI) of approximately 18-30 kg/m2 diagnosed with stageI hypertension
  • Essential Hypertension of greater than at least 1 month duration.
  • 4) Stage 1 Hypertension with Systolic BP 140-159 or Diastolic BP 90-99 (JNC-7 Criteria) of greater than at least 1 month duration

排除标准

  • 1)Secondary Hypertension.
  • 2)Uncontrolled Hypertension.
  • 3)History of Hypersensitivity to Beta Blockers or any component of the product.
  • 4)Patients With Severe Bradycardia, Heart Block, Cardiogenic Shock, Decompensated Heart Failure, Sick Sinus Syndrome.
  • 5)Females who are Pregnant or Lactating or planning to become Pregnant.
  • 8)Subjects on Fluoxetine, Nicardipine, Cimetidine, Non- Dihydropyridine CCB?s and other CYP2D6 Inhibitors.

研究者

发起方
izams Institute of Medical Sciences

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