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Treatment of Hypertension In Adults With ThiaZIDES: Pragmatic Trial Pilot Study (ThiaZIDES)

2017年10月10日 更新者:HealthPartners Institute
This proposed pilot study will test methods and feasibility for a large pragmatic clinical trial comparing two inexpensive, first-line drugs for treating high blood pressure to determine if one is superior in preventing serious cardiovascular events and death. It will develop and test novel approaches to conducting trials that will be faster, less expensive, and more realistic by being embedded in a typical practice setting and using advanced health information technology.

研究概览

详细说明

For several decades, U.S. hypertension treatment guidelines have recommended a low-dose diuretic such as hydrochlorothiazide (HCTZ) or chlorthalidone (CTD) as initial monotherapy in a stepped-care approach or as part of an initial two-drug combination. In numerous large clinical trials, CTD-based regimens have significantly reduced rates of cardiovascular events such as stroke, heart failure, and cardiovascular mortality compared with placebo, usual care, or active comparators. In contrast, few outcome studies have compared HCTZ-based regimens with other treatments, and they have generally found HCTZ to be less effective than non-thiazide comparators in preventing cardiovascular events. The two drugs have never been compared directly in a large trial. Despite the empirical evidence favoring CTD, HCTZ is much more widely used in clinical practice. The proposed R34 is a pilot study conducted in two large integrated health systems to test methods and feasibility for an eventual pragmatic randomized trial comparing the effectiveness of HCTZ and CTD for preventing cardiovascular events and mortality. Using a cluster-randomized design, investigators will allocate 40 primary care physicians and their adult hypertensive patients who currently use HCTZ (N=2,000) to either convert HCTZ users to CTD (intervention group) or to continue HCTZ (usual care group). The pilot study and planned full-scale trial will use existing health care infrastructure and electronic health records to identify eligible study subjects, distribute study medication, and collect operational and outcomes data. For this pilot study, Aim 1 will document that the intervention is delivered as intended. Aim 2 will compare safety in intervention and usual care patients. Aim 3 will refine the pilot study design and identify critical factors for intervention success using a mixed-methods approach. Aim 4 will refine estimates of sample size. Finally, Aim 5 will determine the costs of ascertaining outcomes and estimate per-participant costs for the full-scale trial. The pilot study will produce data that are necessary and sufficient to inform the planning of a full-scale trial comparing CTD and CTZ and will advance the development of methods for pragmatic trials.

研究类型

介入性

注册 (实际的)

2027

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Minnesota
      • Bloomington、Minnesota、美国、55105
        • HealthPartners Institute for Education and Research
    • Oregon
      • Portland、Oregon、美国、97227
        • Kaiser Permanente Center for Health Research

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Adults 18 years and older
  • Hypertension diagnosis (ICD-9 401.x)
  • Current prescription for hydrochlorothiazide (HCTZ), 12.5-50 mg/day as a single-agent (not part of a fixed-dose combination drug)
  • No history of intolerance to chlorthalidone (CTD)
  • No known low levels of sodium (<135 mEg/L (milliequivalents per liter)) or potassium (<3.5 mEg/L)
  • English speaking

Exclusion Criteria:

  • Physician deems patient inappropriate for switching HCTZ to CTD
  • Patient refuses the switch prior to intervention

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Intervention
Intervention is HCTZ prescription conversion to chlorthalidone. Intervention patients are defined as patients of physicians randomized to "intervention." All these patients will have their current prescription of hydrochlorothiazide (HCTZ) switched to an equipotent dose of Chlorthalidone. These patients can choose to decline this intervention, and will be followed for 9 months with no other intervention to observe primary and secondary outcomes.
The intervention is simply a prescription conversion and the main outcome is whether or not patients accept the conversion and treatment with chlorthalidone.
无干预:Usual Care
Usual care patients are defined as patients of physicians randomized to "usual care." All these patients will keep their current prescription for HCTZ and work with their physician like normal. These patients will be followed for 9 months with no intervention to compare primary and secondary outcomes to the intervention group.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Conversion to chlorthalidone, number of patients with primary fills
大体时间:3 months
We will observe pharmacy claims to assess whether intervention patients filled their first prescription for chlorthalidone (primary adherence)
3 months
Conversion to chlorthalidone, number of participants with secondary fills
大体时间:9 months
We will observe pharmacy claims to assess whether intervention patients who filled their first chlorthalidone prescription also filled their subsequent prescription (secondary adherence)
9 months

次要结果测量

结果测量
措施说明
大体时间
Blood pressure
大体时间:9 months
Systolic and diastolic blood pressure measures, as documented in electronic health record
9 months
Hypertension drugs
大体时间:9 months
Use of anti-hypertensive drugs in addition to hydrochlorothiazide or chlorthalidone, as documented in pharmaceutical claims
9 months
Electrolyte levels
大体时间:9 months
Sodium and potassium levels, as documented in electronic health record
9 months
Renal function
大体时间:9 months
Kidney function lab values (including epidermal growth factor receptor (eGFR) and creatinine), as documented in electronic health record
9 months
Safety outcomes
大体时间:9 months
Hypotension with fainting (over-treatment), hypertensive crisis (under-treatment) and other clinical outcomes related to safety of hypertension treatment
9 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

合作者

调查人员

  • 首席研究员:Karen L Margolis, MD, MPH、HealthPartners Institute
  • 首席研究员:Stephen P Fortmann, MD、Kaiser Permanente

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2015年8月1日

初级完成 (实际的)

2017年7月1日

研究完成 (实际的)

2017年7月1日

研究注册日期

首次提交

2015年9月25日

首先提交符合 QC 标准的

2015年10月28日

首次发布 (估计)

2015年10月29日

研究记录更新

最后更新发布 (实际的)

2017年10月11日

上次提交的符合 QC 标准的更新

2017年10月10日

最后验证

2017年1月1日

更多信息

与本研究相关的术语

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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