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临床试验/EUCTR2007-005655-42-GB
EUCTR2007-005655-42-GB进行中(未招募)1 期

STUDY TITLE: - Early Metabolic Changes with Thiazide or Beta blocker Therapy for Essential Hypertension – open label extension phase with the potassium sparing diuretic- Amiloride.

Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital0 个研究点目标入组 0 人开始时间: 2008年3月19日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

入选标准

  • Our ongoing, previously approved study is a double-blind, placebo controlled, cross-over study, of approximately 66 patients in which each patient receives in random order, 4 weeks treatment with either Bendrofluazide 5-10mg daily, Atenolol 50-100mg daily or combination of Bendrofluazide 2.5-5.0mg and Atenolol 25-50mg daily.
  • Patients who have completed the main part of the study will be invited to take part in an open label phase with 10mg of amiloride for 2 weeks increasing to 20mg amiloride for 2 weeks.
  • Are the trial subjects under 18?
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • All patients will have taken part in the previous study and the original exclusion criteria still therefore stand:
  • Any patient already taking thiazide diuretics or beta blockers in whom these drugs cannot be switched to alternative drugs with similar or better blood pressure control.
  • Any patient who is intolerant of these medications will be excluded from the study.
  • Patients with gout, asthma or any other contraindications to the study drugs will be excluded.
  • Women of child bearing age not using contraception.
  • Volunteers with heart failure, liver failure, renal failure, terminal illnesses (e.g. cancer)
  • Volunteers not able to give informed consent
  • Patients with diabetes
  • New exclusion criteria include:
  • Patients with plasma potassium over 5.5mmol/l, concomitant use of other potassium sparing agents or potassium supplements, anuria, acute renal failure, severe progressive renal disease (ie patients at highest risk of hyperkalaemia) would all be excluded from this study.

研究者

发起方
Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital

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