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Bypass Angioplasty Revascularization Investigation in Type 2 Diabetes (BARI2D)

2016年1月12日 更新者:Maria Mori Brooks、University of Pittsburgh

The BARI 2D trial is a multicenter study that uses a 2x2 factorial design, with 2400 patients being assigned at random to initial elective revascularization with aggressive medical therapy or aggressive medical therapy alone with equal probability, and simultaneously being assigned at random to an insulin providing or insulin sensitizing strategy of glycemic control (with a target value for HbA1c of less than 7.0% for all patients).

SPECIFIC AIMS

A. Primary Aim

The primary aim of the BARI 2D trial is to test the following two hypotheses of treatment efficacy in 2400 patients with Type 2 diabetes mellitus and documented stable CAD, in the setting of uniform glycemic control and intensive management of all other risk factors including dyslipidemia, hypertension, smoking, and obesity:

  1. Coronary Revascularization Hypothesis: a strategy of initial elective revascularization of choice (surgical or catheter-based) combined with aggressive medical therapy results in lower 5-year mortality compared to a strategy of aggressive medical therapy alone;
  2. Method of Glycemic Control Hypothesis: with a target HbA1c level of less than 7.0%, a strategy of hyperglycemia management directed at insulin sensitization results in lower 5-year mortality compared to a strategy of insulin provision.

B. Secondary Aims

The secondary aims of the BARI 2D trial include: a) comparing the death, myocardial infarction or stroke combined endpoint event rate between the revascularization versus medical therapy groups and between the insulin sensitization versus insulin provision groups; b) comparing rates of myocardial infarction, other ischemic events, angina and quality of life associated with each revascularization and hyperglycemia management strategy; c) evaluating the relative economic costs associated with the trial treatment strategies, d) exploring the effect of glycemic control strategy on the progression and mechanism of vasculopathy including changes in PAI-1 gene expression.

調査の概要

詳細な説明

BACKGROUND:

Type 2 diabetes mellitus, which is becoming more prevalent in our society as the population ages, is one of the strongest risk factors for coronary artery disease (CAD) and consequent mortality. In addition to generating an enormous toll in human suffering, diabetes places an economic burden approaching 100 billion dollars annually on the U.S. health care system. Despite the well known dismal prognosis of diabetes complicated by angiographically documented CAD, the optimal treatment paradigm for this large group of patients has not been studied. Coronary revascularization, while increasingly used, has not been directly shown to be of additional benefit to simultaneous intensive medical management of CAD along with management of hyperglycemia, hypertension, dyslipidemia, and other risk factors. Moreover, while intensive efforts to lower HbA1c have been demonstrated to favorably affect the clinical course of Type 2 diabetes mellitus in terms of microvascular complications, the optimal hyperglycemia management strategy with regard to macrovascular outcome is not known.

These critical treatment dilemmas have motivated the development of BARI 2D, a multicenter randomized trial designed to determine in patients with Type 2 diabetes and stable CAD: 1) the efficacy of initial elective coronary revascularization combined with aggressive medical therapy, compared to an initial strategy of aggressive medical therapy alone; and 2) the efficacy of a strategy of providing more insulin (endogenous or exogenous), versus a strategy of increasing sensitivity to insulin (reducing insulin resistance), in the management of hyperglycemia, with a target HbA1c level of less than 7.0% for each strategy.

DESIGN NARRATIVE:

The BARI 2D trial is a multicenter study that uses a 2x2 factorial design, with 2400 patients being assigned at random to initial elective revascularization with aggressive medical therapy or aggressive medical therapy alone with equal probability, and simultaneously being assigned at random to an insulin providing or insulin sensitizing strategy of glycemic control (with a target value for HbA1c of less than 7.0% for all patients). Following confirmation of patient eligibility and provision of written consent, patients were randomized as shown below:

Number of Patients Per Treatment Assignment (N=2400 patients in total)

Stable Ischemic Heart Disease Treatment Strategy and Glycemic Control Strategy:

Revascularization and Insulin Providing (IP) N=600; Revascularization and Insulin Sensitizing (IS) N=600; Medical and Insulin Providing (IP) N=600; Medical and and Insulin Sensitizing (IS) N=600.

研究の種類

介入

入学 (実際)

2368

段階

  • フェーズ 3

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

25年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Diagnosis of Type 2 diabetes mellitus
  • Coronary arteriogram showing one or more vessels amenable to revascularization (greater than or equal to 50% stenosis)
  • Objective documentation of ischemia OR subjectively documented typical angina with greater than or equal to 70% stenosis in at least one artery
  • Suitability for coronary revascularization by at least one of the available methods (does not require the ability to achieve complete revascularization)
  • Ability to perform all tasks related to glycemic control and risk factor management

Exclusion Criteria:

  • Definite need for invasive intervention as determined by the attending cardiologist
  • Prior bypass surgery (CABG) or prior catheter-based intervention within the 12 months before study entry
  • Planned intervention for disease in bypass graft(s) if the patient is randomly assigned to a strategy of initial revascularization
  • Class III or IV CHF
  • Creatinine greater than 2.0 mg/dL
  • HbA1c greater than 13%
  • Need for major vascular surgery concomitant with revascularization (e.g., carotid endarterectomy)
  • Left main stenosis greater than or equal to 50%
  • Non-cardiac illness expected to limit survival
  • Hepatic disease (ALT greater than 2 times the ULN)
  • Fasting triglycerides greater than 1000 mg/dL in the presence of moderate glycemic control (HbA1c less than 9.0%)
  • Current alcohol abuse
  • Chronic steroid use judged to interfere with the control of diabetes, exceeding 10 mg of Prednisone per day or the equivalent
  • Pregnancy, known, suspected, or planned in 5 years after study entry
  • Geographically inaccessible or unable to return for follow-up
  • Enrolled in a competing randomized trial or clinical study
  • Unable to understand or cooperate with protocol requirements

Patients with Type 2 diabetes mellitus and CAD documented by coronary arteriography will be eligible for the trial if revascularization is not required for prompt control of severe or unstable angina. Diabetic patients who are being treated with insulin or oral hypoglycemic drugs will be eligible as well as diabetic patients treated with diet and exercise alone provided that a diagnosis of diabetes can be confirmed by record review or that a fasting plasma glucose (FPG) greater than 125/mg/dL (7.0 mmol/L) can be obtained. The determination of suitability for BARI 2D will be made by a physician-investigator at each participating institution on clinical grounds at the time of coronary angiography.

Significant CAD will be defined as at least one stenosis greater than 50%. Angina and ischemia will be assessed by use of patient self-report, physician examination, and appropriate diagnostic measures including exercise myocardial perfusion imaging, exercise echocardiography, exercise electrocardiography, and IV dipyridamole or adenosine myocardial perfusion imaging or invasively by doppler or pressure wire. Objective documentation of myocardial ischemia includes any of the following:

  1. Exercise or pharmacologically-induced:

    1. Greater than or equal to 1 mm of horizontal or downsloping ST depression or elevation for greater than or equal to 60-80 milliseconds after the end of the QRS complex
    2. Myocardial perfusion defect
    3. Myocardial wall motion abnormality
  2. Stabilized, prior acute coronary syndrome with CK-MB or troponin elevation or with new, greater than or equal to 0.5 mm ST depression or elevation, or T wave inversion of greater than or equal to 3 mm in 2 contiguous ECG leads
  3. Doppler or pressure wire showing coronary flow reserve (CFR) less than 2.0 or fractional flow reserve (FFR) less than 0.75

Among patients without documented ischemia, only patients with stenosis greater than or equal to 70% presenting with classic anginal symptoms will be eligible for randomization.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:階乗代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ:Revascularization and Insulin Providing (IP)
Prompt revascularization with intensive medical therapy and insulin providing glycemic control strategy
Angioplasty, Transluminal, Percutaneous Coronary, other catheter-based interventions
Coronary Artery Bypass
Insulin, sulfonylurea
ACE Inhibitors, Angiotensin Receptor Blockers, Beta Blockers, Calcium Channel Blockers
アクティブコンパレータ:Revascularization and Insulin Sensitizing (IS)
Prompt revascularization with intensive medical therapy and insulin sensitizing glycemic control strategy
Angioplasty, Transluminal, Percutaneous Coronary, other catheter-based interventions
Coronary Artery Bypass
ACE Inhibitors, Angiotensin Receptor Blockers, Beta Blockers, Calcium Channel Blockers
Biguanides, thiazolidinediones
アクティブコンパレータ:Medical Therapy and Insulin Providing (IP)
Intensive medical therapy with delayed revascularization if clinically indicated and insulin providing glycemic control strategy
Insulin, sulfonylurea
ACE Inhibitors, Angiotensin Receptor Blockers, Beta Blockers, Calcium Channel Blockers
アクティブコンパレータ:Medical Therapy and Insulin Sensitizing (IS)
Intensive medical therapy with delayed revascularization if clinically indicated and insulin sensitizing glycemic control strategy
ACE Inhibitors, Angiotensin Receptor Blockers, Beta Blockers, Calcium Channel Blockers
Biguanides, thiazolidinediones

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
Number of Participants With All-Cause Mortality
時間枠:five years
five years

二次結果の測定

結果測定
時間枠
Number of Participants With Death, Myocardial Infarction, or Stroke
時間枠:five years
five years

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Bernard Chaitman, MD、St. Louis University
  • スタディチェア:Robert L Frye, MD、Mayo Clinic
  • 主任研究者:Mark Hlatky、Stanford University
  • 主任研究者:Burton Sobel、University of Vermont & State Agricultural College
  • 主任研究者:Sheryl F. Kelsey, PhD、University of Pittsburgh

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2000年9月1日

一次修了 (実際)

2008年11月1日

研究の完了 (実際)

2009年3月1日

試験登録日

最初に提出

2000年9月28日

QC基準を満たした最初の提出物

2000年9月28日

最初の投稿 (見積もり)

2000年9月29日

学習記録の更新

投稿された最後の更新 (見積もり)

2016年2月8日

QC基準を満たした最後の更新が送信されました

2016年1月12日

最終確認日

2016年1月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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