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Prediction of Findings From the Ongoing CAROLINA Trial Using Healthcare Database Analyses

2020年9月23日 更新者:Elisabetta Patorno、Brigham and Women's Hospital
This cohort study was initiated to predict the findings of CAROLINA trial in a real world setting using electronic claims data from insurance databases with results anticipated prior to the completion of CAROLINA.

研究概览

地位

完全的

详细说明

The CARdiovascular Outcome Trial of LINAgliptin Versus Glimepiride in Type 2 Diabetes (CAROLINA) is an ongoing randomized controlled trial (RCT) designed to assess whether linagliptin is non-inferior, and if so, superior compared with glimepiride 1-4 mg once daily with respect to cardiovascular (CV) events in adults with relatively early Type 2 Diabetes at increased risk of CV events and with less than optimized glycaemic control. Given that medications of both classes are currently advocated as second-line therapy after metformin, and since sulfonylureas have been associated with concerns regarding their CV safety, while dipeptidyl peptidase-4 inhibitors have been suggested to exhibit CV benefits in preclinical and mechanistic trials, the results of this trial will provide answers to several clinically relevant questions and have a significant impact on clinical practice.

This cohort study was initiated to predict the findings of CAROLINA trial in a real world setting using electronic claims data from insurance databases with results anticipated prior to the completion of CAROLINA. Trial eligibility criteria were adapted in claims data to generate a comparable study cohort (of linagliptin and glimepiride initiators) to that of the trial population. Using 1:1 propensity score-matching was used to control for >120 baseline characteristics. Patients were followed up for a composite cardiovascular outcome adapted from the primary end-point of the CAROLINA trial.

研究类型

观察性的

注册 (实际的)

48262

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

    • Massachusetts
      • Boston、Massachusetts、美国、02120
        • Brigham and Women's Hospital

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

40年 至 85年 (成人、年长者)

接受健康志愿者

不适用

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Patients 40 - 85 years of age with early Type 2 Diabetes mellitus, increased cardiovascular risk or established complications

描述

Inclusion Criteria:

  • Patients with Type 2 diabetes who were new users of Linagliptin or new users of Glimepiride and:

    - Had no more than 3 anti-diabetic drugs including index drug

  • AND at elevated risk of cardiovascular (CV) events according to specific criteria:

    • Previous vascular disease
    • Evidence of vascular-related end-organ damage
    • Age ⩾ 70 years
    • ⩾ 2 CV risk factors:

      • Treated hypertension
      • Smoking
      • Using any lipid lowering treatment
  • Age ≥ 40 and ≤ 85 years at treatment initiation

Exclusion Criteria:

  • Patients with Type 1 Diabetes Mellitus
  • Previous exposure to dipeptidyl peptidase-4 (DPP-4) inhibitors, glucagon-like peptide-1 (GLP-1) receptor agonists, thiazolidinediones (TZDs), insulin or sodium glucose co-transporter-2 (SGLT-2s).
  • Exclude anti-diabetic background therapy if initiated in 2 months prior
  • Morbid obesity or treatment with anti-obesity drugs 3 months prior to treatment initiation
  • Severe hyperglycemia
  • Active liver disease or impaired hepatic function
  • Any previous bariatric surgery
  • Coronary artery re-vascularisation ≤ 6 weeks prior to treatment initiation
  • Prior hospitalization for congestive heart failure
  • Acute or chronic metabolic acidosis
  • Hereditary galactose intolerance
  • Alcohol or drug abuse within the 3 months prior to treatment initiation
  • Use of oral corticosteroids
  • Pregnant women
  • Patients with cancer
  • Acute coronary syndrome ≤ 6 weeks prior to treatment initiation
  • Stroke or Transient ischemic attack ≤ 3 months prior to treatment initiation

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

队列和干预

团体/队列
Linagliptin
Patients who initiate Linagliptin with no use in the prior 180 days
Glimepiride
Patients who initiate Glimepiride with no use in the prior 180 days

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
Composite Cardiovascular (CV) Outcome
大体时间:From treatment initiation to end of follow-up, up to 53 months
Composite CV Outcome includes Myocardial infarction, Stroke, hospitalization for unstable angina and Death
From treatment initiation to end of follow-up, up to 53 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。

调查人员

  • 首席研究员:Elisabetta Patorno, MD DrPH、Brigham and Women's Hospital, Harvard Medical School

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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 (实际的)

2011年5月1日

初级完成 (实际的)

2019年6月1日

研究完成 (实际的)

2019年6月1日

研究注册日期

首次提交

2018年8月24日

首先提交符合 QC 标准的

2018年8月24日

首次发布 (实际的)

2018年8月27日

研究记录更新

最后更新发布 (实际的)

2020年9月25日

上次提交的符合 QC 标准的更新

2020年9月23日

最后验证

2020年9月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

在美国制造并从美国出口的产品

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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