Prevention of Events With Angiotensin-Converting Enzyme Inhibitor Therapy (PEACE) - Catalog
Prevention of Events With Angiotensin-Converting Enzyme Inhibitor Therapy (PEACE)
HLB00620823a
PEACE
PEC
False
True
True
Coded
False
Clinical Trial
Open BioLINCC Study
Adult
Drug: angiotensin-converting enzyme inhibitors
2009-10-01
2009-10-01
2008-10-13
2008-01-15
November 1995 - June 2005
DCVS
Heart
non-HIV
non-COVID
0
0
No
No
No
Yes
Yes
Yes
Consent restricts use of biospecimens to research related to predictors of coronary heart disease progression.
Cardiovascular Diseases
Coronary Disease
Heart Diseases
Myocardial Infarction
Myocardial Ischemia
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.
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.
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).
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)
Plasma
Serum
Urine
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
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Material Types
-
General Freeze/Thaw Status
-
Visits (Vials)25 July 2023
Last Modified: July 25, 2023, 11:57 a.m. -
Visits (Subjects)25 July 2023
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.