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Bypass Angioplasty Revascularization Investigation in Type 2 Diabetes (BARI2D)

2016. január 12. frissítette: 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.

A tanulmány áttekintése

Részletes leírás

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.

Tanulmány típusa

Beavatkozó

Beiratkozás (Tényleges)

2368

Fázis

  • 3. fázis

Részvételi kritériumok

A kutatók olyan embereket keresnek, akik megfelelnek egy bizonyos leírásnak, az úgynevezett jogosultsági kritériumoknak. Néhány példa ezekre a kritériumokra a személy általános egészségi állapota vagy a korábbi kezelések.

Jogosultsági kritériumok

Tanulmányozható életkorok

25 év és régebbi (Felnőtt, Idősebb felnőtt)

Egészséges önkénteseket fogad

Nem

Tanulmányozható nemek

Összes

Leírás

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.

Tanulási terv

Ez a rész a vizsgálati terv részleteit tartalmazza, beleértve a vizsgálat megtervezését és a vizsgálat mérését.

Hogyan készül a tanulmány?

Tervezési részletek

  • Elsődleges cél: Kezelés
  • Kiosztás: Véletlenszerűsített
  • Beavatkozó modell: Tényező hozzárendelés
  • Maszkolás: Nincs (Open Label)

Fegyverek és beavatkozások

Résztvevő csoport / kar
Beavatkozás / kezelés
Aktív összehasonlító: 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
Aktív összehasonlító: 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
Aktív összehasonlító: 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
Aktív összehasonlító: 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

Mit mér a tanulmány?

Elsődleges eredményintézkedések

Eredménymérő
Időkeret
Number of Participants With All-Cause Mortality
Időkeret: five years
five years

Másodlagos eredményintézkedések

Eredménymérő
Időkeret
Number of Participants With Death, Myocardial Infarction, or Stroke
Időkeret: five years
five years

Együttműködők és nyomozók

Itt találhatja meg a tanulmányban érintett személyeket és szervezeteket.

Nyomozók

  • Kutatásvezető: Bernard Chaitman, MD, St. Louis University
  • Tanulmányi szék: Robert L Frye, MD, Mayo Clinic
  • Kutatásvezető: Mark Hlatky, Stanford University
  • Kutatásvezető: Burton Sobel, University of Vermont & State Agricultural College
  • Kutatásvezető: Sheryl F. Kelsey, PhD, University of Pittsburgh

Publikációk és hasznos linkek

A vizsgálattal kapcsolatos információk beviteléért felelős személy önkéntesen bocsátja rendelkezésre ezeket a kiadványokat. Ezek bármiről szólhatnak, ami a tanulmányhoz kapcsolódik.

Általános kiadványok

Tanulmányi rekorddátumok

Ezek a dátumok nyomon követik a ClinicalTrials.gov webhelyre benyújtott vizsgálati rekordok és összefoglaló eredmények benyújtásának folyamatát. A vizsgálati feljegyzéseket és a jelentett eredményeket a Nemzeti Orvostudományi Könyvtár (NLM) felülvizsgálja, hogy megbizonyosodjon arról, hogy megfelelnek-e az adott minőség-ellenőrzési szabványoknak, mielőtt közzéteszik őket a nyilvános weboldalon.

Tanulmány főbb dátumok

Tanulmány kezdete

2000. szeptember 1.

Elsődleges befejezés (Tényleges)

2008. november 1.

A tanulmány befejezése (Tényleges)

2009. március 1.

Tanulmányi regisztráció dátumai

Először benyújtva

2000. szeptember 28.

Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak

2000. szeptember 28.

Első közzététel (Becslés)

2000. szeptember 29.

Tanulmányi rekordok frissítései

Utolsó frissítés közzétéve (Becslés)

2016. február 8.

Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak

2016. január 12.

Utolsó ellenőrzés

2016. január 1.

Több információ

Ezt az információt közvetlenül a clinicaltrials.gov webhelyről szereztük be, változtatás nélkül. Ha bármilyen kérése van vizsgálati adatainak módosítására, eltávolítására vagy frissítésére, kérjük, írjon a következő címre: register@clinicaltrials.gov. Amint a változás bevezetésre kerül a clinicaltrials.gov oldalon, ez a webhelyünkön is automatikusan frissül. .

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