Prevention of Events With Angiotensin-Converting Enzyme Inhibitor Therapy (PEACE) - Catalog

Name

Prevention of Events With Angiotensin-Converting Enzyme Inhibitor Therapy (PEACE)

Accession Number

HLB00620823a

Acronym

PEACE

Related studies

BSI Study IDs

PEC

Is public use dataset

False

Keywords

Has Study Datasets

True

Has Specimens

True

Specimen ID Type

Coded

Study Website

The Framingham Heart Study Group requires that the requestor must obtain full or expedited IRB/Ethics Committee review and approval to obtain these data. Waivers or a determination that the research is exempt from ethical regulations do not suffice.

False

Study type

Clinical Trial

Collection Type

Open BioLINCC Study

Cohort type

Adult

Interventions

Drug: angiotensin-converting enzyme inhibitors

Study Open Date (Data)

2009-10-01

Study Open Date (Specimens)

2009-10-01

Date materials available

2008-10-13

Last updated

2008-01-15

Study period

November 1995 - June 2005

Study Contacts
NHLBI Division

DCVS

Classification

Heart

HIV study classification

non-HIV

COVID study classification

non-COVID

Pre-Website # of Specimens Shipped

0

# of Returned Specimens

0

Conditions

Cardiovascular Diseases
Coronary Disease
Heart Diseases
Myocardial Infarction
Myocardial Ischemia

Objectives

To conduct a trial to test the hypothesis that patients with stable coronary artery disease and normal or slightly reduced left ventricular function derive therapeutic benefit from the addition of ACE inhibitors to modern conventional therapy.

Background

Angiotensin-converting-enzyme (ACE) inhibitors are effective in reducing the risk of heart failure, myocardial infarction, and death from cardiovascular causes in patients with left ventricular systolic dysfunction or heart failure. ACE inhibitors have also been shown to reduce atherosclerotic complications in patients who have vascular disease without heart failure.

Participants

The trial was a double-blind, placebo-controlled study in which 8290 patients were randomly assigned to receive either trandolapril at a target dose of 4 mg per day (4158 patients) or matching placebo (4132 patients).

Design

Conclusions

In patients with stable coronary heart disease and preserved left ventricular function who are receiving "current standard" therapy and in whom the rate of cardiovascular events is lower than in previous trials of ACE inhibitors in patients with vascular disease, there is no evidence that the addition of an ACE inhibitor provides further benefit in terms of death from cardiovascular causes, myocardial infarction, or coronary revascularization. (NEJM 2004;351:2058-2068)

Disease classification

Publications

Mat types

Plasma
Serum
Urine

Network

The study population available in BioLINCC study data may be lower than total study enrollment due to Informed Consent restrictions and other factors.

  • Subjects

    Placebo: 4,132

    Active Drug, Trandolapril: 4,158


    Last Modified: March 8, 2016, 12:16 p.m.
  • Age

     

    Placebo

    Active drug, trandolapril

    All

    N

    %

    N

    %

    N

    %

    46-50

    91

    2.20

    94

    2.26

    185

    2.23

    51-55

    610

    14.76

    629

    15.13

    1239

    14.95

    56-60

    781

    18.90

    733

    17.63

    1514

    18.26

    61-65

    817

    19.77

    803

    19.31

    1620

    19.54

    66-70

    795

    19.24

    868

    20.88

    1663

    20.06

    71-75

    621

    15.03

    620

    14.91

    1241

    14.97

    76-80

    349

    8.45

    332

    7.98

    681

    8.21

    >=81

    68

    1.65

    79

    1.90

    147

    1.77

     

    Last Modified: Aug. 25, 2015, 3:50 p.m.
  • Sex
     

     

    Placebo

    Active drug, trandolapril

    All

    N

    %

    N

    %

    N

    %

    Female

    704

    17.04

    790

    19.00

    1494

    18.02

    Male

    3428

    82.96

    3368

    81.00

    6796

    81.98

     

    Last Modified: Aug. 25, 2015, 3:50 p.m.
  • Race

Please note that biospecimen availability is subject to review by the NHLBI, BioLINCC, and the NHLBI Biorepository. Certain biospecimens may not be made available for your request. Section 3 of the BioLINCC handbook describes the components of the review process

  • Material Types
  • General Freeze/Thaw Status
  • Visits (Vials)
    25 July 2023
     
    Serum Plasma Urine Total
    Baseline 7,359 21,256 6,712 35,327
    Follow-up Visit 1 55 79 35 169
    Follow-up Visit 2 1,244 1,561 724 3,529
    Follow-up Visit 3 701 889 388 1,978
    Follow-up Visit 4 1,823 2,312 1,002 5,137
    Follow-up Visit 5 1,017 1,276 545 2,838
    Follow-up Visit 6 2,820 3,517 1,546 7,883
    Follow-up Visit 7 1,274 1,644 675 3,593
    Follow-up Visit 8 2,220 2,783 1,232 6,235
    Follow-up Visit 9 427 561 230 1,218
    Follow-up Visit 10 423 585 238 1,246
    Follow-up Visit 11 110 154 57 321
    Follow-up Visit 12 29 38 18 85
    Unknown 1,511 2,097 736 4,344

    Last Modified: July 25, 2023, 11:57 a.m.
  • Visits (Subjects)
    25 July 2023
     
    Serum
    Total number of subjects Average volume (ml) per subject
    Baseline 3,701 0.99
    Follow-up Visit 1 13 2.12
    Follow-up Visit 2 251 2.48
    Follow-up Visit 3 141 2.49
    Follow-up Visit 4 369 2.49
    Follow-up Visit 5 207 2.49
    Follow-up Visit 6 571 2.47
    Follow-up Visit 7 258 2.49
    Follow-up Visit 8 450 2.48
    Follow-up Visit 9 86 2.67
    Follow-up Visit 10 86 2.63
    Follow-up Visit 11 22 2.50
    Follow-up Visit 12 6 2.42
    Unknown 306 2.48
     
      Plasma
    Total number of subjects Average volume (ml) per subject
    Baseline 3,770 1.94
    Follow-up Visit 1 13 2.98
    Follow-up Visit 2 251 3.17
    Follow-up Visit 3 140 3.25
    Follow-up Visit 4 368 3.13
    Follow-up Visit 5 208 3.03
    Follow-up Visit 6 573 3.12
    Follow-up Visit 7 260 3.24
    Follow-up Visit 8 450 3.23
    Follow-up Visit 9 87 3.58
    Follow-up Visit 10 86 3.50
    Follow-up Visit 11 22 3.76
    Follow-up Visit 12 6 2.83
    Unknown 306 3.48
     
      Urine
    Total number of subjects Average volume (ml) per subject
    Baseline 3,367 11.32
    Follow-up Visit 1 12 14.58
    Follow-up Visit 2 242 14.96
    Follow-up Visit 3 130 14.92
    Follow-up Visit 4 335 14.96
    Follow-up Visit 5 184 14.81
    Follow-up Visit 6 516 14.98
    Follow-up Visit 7 225 15.00
    Follow-up Visit 8 413 14.92
    Follow-up Visit 9 77 14.94
    Follow-up Visit 10 80 14.88
    Follow-up Visit 11 19 15.00
    Follow-up Visit 12 6 15.00
    Unknown 244 15.30

    Last Modified: July 25, 2023, 11:57 a.m.