跳至主要内容
临床试验/EUCTR2017-004004-22-GB
EUCTR2017-004004-22-GB进行中(未招募)1 期

A Multi-Centred, Open Label, Randomised Study Assessing the Cardiovascular Outcomes Following Treatment of White Coat Hypertension with Established Anti-Hypertensive Drugs versus Standard of Care in the Very Elderly - Feasibility Study - HYVET 2: Treatment of white coat HYpertension in the Very Elderly

niversity of Sussex0 个研究点目标入组 100 人开始时间: 2018年1月18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
入组人数
100

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

性别
All

入选标准

  • Patients =75 years of age
  • Clinic sitting systolic BP =150mmHg but <200mmHg and diastolic BP <110mmHg
  • Diagnosis of white coat hypertension at baseline if the mean ambulatory day time average systolic BP is <135 mmHg and diastolic BP is <85mmHg (from at least 14 measurements) or for HBPM from BP readings twice a day for at least 5 days (ideally 7 days)at baseline
  • Not taken antihypertensive drug therapy within the last 6 months
  • Capacity to consent
  • Provision of documented informed consent
  • Ability to comply with the protocol and additional study visits & assessments
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range 0
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 100

排除标准

  • Contraindication to the use of indapamide MR and perindopril in accordance with the summary of product characteristics
  • Regular non-steroidal anti-inflammatory drug (NSAID) use. Regular use being defined by the local GP with consideration to cardiovascular risk and blood pressure
  • Hypertensive emergency
  • Secondary hypertension
  • Postural hypotension (postural drop in systolic BP=20mmHg or postural symptoms at screening)
  • Any stroke or myocardial infarction in the previous 6 months
  • Heart failure requiring treatment with drugs having an antihypertensive effect
  • Previous documented evidence of gout
  • eGFR less than 30ml/min
  • Montreal cognitive assessment score (MoCA) < 22
  • Life expectancy <1year due to malignancy or chronic disease

研究者

发起方
niversity of Sussex

相似试验

进行中(未招募)
不适用
HYVET 2: treatment of white coat hypertension in the very elderlyWhite coat hypertension
ISRCTN13127656niversity of Sussex100
进行中(未招募)
1 期
A study to assess the pharmacokinetics, safety, and efficacy of two doses of bimekizumab in adolescent study participants with moderate to severe plaque psoriasisModerate to Severe Plaque PsoriasisMedDRA version: 20.0Level: LLTClassification code 10071117Term: Plaque psoriasisSystem Organ Class: 100000004858
EUCTR2020-001724-34-DECB Biopharma SR40
进行中(未招募)
1 期
A study to assess the pharmacokinetics, safety, and efficacy of two doses of bimekizumab in adolescent study participants with moderate to severe plaque psoriasisModerate to Severe Plaque PsoriasisMedDRA version: 20.0Level: LLTClassification code 10071117Term: Plaque psoriasisSystem Organ Class: 100000004858
EUCTR2020-001724-34-Outside-EU/EEACB Biopharma SR
进行中(未招募)
1 期
A study to assess the pharmacokinetics, safety, and efficacy of two doses of bimekizumab in adolescent study participants with moderate to severe plaque psoriasisModerate to Severe Plaque PsoriasisMedDRA version: 20.0Level: LLTClassification code 10071117Term: Plaque psoriasisSystem Organ Class: 10040785 - Skin and subcutaneous tissue disorders
EUCTR2020-001724-34-PLCB Biopharma SR40
进行中(未招募)
1 期
A study to learn how safe bimekizumab, how well it works and how it moves through the bloodstream in adolescents with moderate to severe plaque psoriasisModerate to Severe Plaque PsoriasisMedDRA version: 20.0Level: LLTClassification code: 10071117Term: Plaque psoriasis Class: 10040785
CTIS2023-509832-24-00CB Biopharma43