Related trials
CSPPT, 2015 - folic acid vs placebo
VITATOPS, 2010 - folic acid, vit B12 and vit B6 vs placebo
WAFACS, 2008 - folic acid, vit B12 and vit B6 vs placebo
WENBIT (vit B6), 2008 - vit B6 vs placebo
WENBIT (folic ac,B12), 2008 - folic acid, B12 vs placebo
SEARCH, 2007 - folic acid, B12 vs placebo
NORVIT (folic acid + B12) (Bonaa), 2006 - folic acid, B12 vs control
NORVIT (folic acid, B12 and vit B6) (Bonaa), 2006 - folic acid, vit B12 and vit B6 vs control
NORVIT (vit B6) (Bonaa), 2006 - vit B6 vs control
HOPE-2 (Lonn), 2006 - folic acid, vit B12 and vit B6 vs placebo
FOLARDA (Liem), 2004 - folic acid vs control
VISP (Toole), 2004 - high dose - folic acid, vit B12 and vit B6 vs low dose - folic acid, vit B12 and vit B6
GOES (Liem), 2003 - folic acid vs control
CHAOS-2, 2002 - folic acid vs placebo
SU.FOL.OM3, - folic acid, vit B12 and vit B6 vs placebo
See also:
All cardiovascular prevention clinical trials
All clinical trials of plasma homocysteine lowering intervention
All clinical trials of folic acid
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|
Treatments
Studied treatment |
enalapril 10 mg / folic acid 0.8 mg daily
|
Control treatment |
Enalapril maleate 10 mg daily
|
Concomittant treatment |
on top enalapril |
Patients
Patients |
patients with primary hypertension |
Method and design
Randomized effectives |
10348 / 10354 (studied vs. control) |
Design |
Parallel groups |
Blinding |
double-blind |
Geographic area |
China |
Primary endpoint |
symptomatic stroke ( ischemic or hemorrhagic) |
Results
Endpoints and data reported in the trial's publication(s)
Endpoint |
Events (%) |
Relative Risk |
95% CI |
|
Studied treat. |
Control treat. |
First stroke |
282 / 10348 (2,7%) |
355 / 10354 (3,4%) |
0,79 |
[0,68;0,93] |
|
Ischemic stroke |
223 / 10348 (2,2%) |
292 / 10354 (2,8%) |
0,76 |
[0,64;0,91] |
|
Hemorrhagic stroke |
58 / 10348 (0,6%) |
62 / 10354 (0,6%) |
0,94 |
[0,66;1,34] |
|
Composite of stroke, myocardial infarction, or death due to cardiovascular causes |
324 / 10348 (3,1%) |
405 / 10354 (3,9%) |
0,80 |
[0,69;0,92] |
|
Myocardial infarctione |
25 / 10348 (0,2%) |
24 / 10354 (0,2%) |
1,04 |
[0,60;1,82] |
|
Death due to cardiovascular causesf |
43 / 10348 (0,4%) |
43 / 10354 (0,4%) |
1,00 |
[0,66;1,53] |
|
All-cause death |
302 / 10348 (2,9%) |
320 / 10354 (3,1%) |
0,94 |
[0,81;1,10] |
|
Endpoints used by the meta-analysis and data retained for this trial
Endpoint
Studied treat. n/N
Control treat. n/N
Graph
RR [95% CI]
All cause death
302 / 10348
320 / 10354
0,94 [0,81;1,10]
Non fatal MI
25 / 10348
24 / 10354
1,04 [0,60;1,82]
cardiovascular events
324 / 10348
405 / 10354
0,80 [0,69;0,92]
Cardiovascular death
43 / 10348
43 / 10354
1,00 [0,66;1,53]
stroke (fatal and non fatal)
282 / 10348
355 / 10354
0,79 [0,68;0,93]
0
2
1.0
Relative risks
|
Endpoint |
Events (%) |
Relative Risk |
95% CI |
Endpoint definition in the trial |
Ref |
Studied treat. |
Control treat. |
All cause death
|
302 / 10348 (2,9%) |
320 / 10354 (3,1%) |
0,94 |
[0,81;1,10] |
All-cause death |
|
Non fatal MI
|
25 / 10348 (0,2%) |
24 / 10354 (0,2%) |
1,04 |
[0,60;1,82] |
Myocardial infarctione |
|
cardiovascular events
|
324 / 10348 (3,1%) |
405 / 10354 (3,9%) |
0,80 |
[0,69;0,92] |
Composite of stroke, myocardial infarction, or death due to cardiovascular causes |
|
Cardiovascular death
|
43 / 10348 (0,4%) |
43 / 10354 (0,4%) |
1,00 |
[0,66;1,53] |
Death due to cardiovascular causesf |
|
stroke (fatal and non fatal)
|
282 / 10348 (2,7%) |
355 / 10354 (3,4%) |
0,79 |
[0,68;0,93] |
First stroke |
|
The primary endpoint (if exists) appears in blod characters
|
Reference(s) used for data extraction:
|
Endpoint |
studied treat. |
control treat. |
mean diff |
Absolute risk reduction (for a follow-up of )
|
Endpoint |
Events rate |
Absolute risk reduction (ARR) |
Studied treat. |
Control treat. |
All cause death |
2,92% |
3,09% |
-0,17%
|
Non fatal MI |
2,42‰ |
2,32‰ |
0,01%
|
cardiovascular events |
3,13% |
3,91% |
-0,78%
|
Cardiovascular death |
4,16‰ |
4,15‰ |
0,00%
|
stroke (fatal and non fatal) |
2,73% |
3,43% |
-0,70%
|
Meta-analysis of all similar trials:
plasma homocysteine lowering intervention in cardiovascular prevention for all type of patients
Reference(s)
TrialResults-center ID |
TRC11319
|
Trials register # |
NCT00794885
|
-
Huo Y, Li J, Qin X, Huang Y, Wang X, Gottesman RF, Tang G, Wang B, Chen D, He M, Fu J, Cai Y, Shi X, Zhang Y, Cui Y, Sun N, Li X, Cheng X, Wang J, Yang X, Yang T, Xiao C, Zhao G, Dong Q, Zhu D, Wang X, Ge J, Zhao L, Hu D, Liu L, Hou FF.
Efficacy of Folic Acid Therapy in Primary Prevention of Stroke Among Adults With Hypertension in China: The CSPPT Randomized Clinical Trial..
JAMA 2015 Mar 15;:
- 10.1001/jama.2015.2274
Pubmed
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Hubmed
| Fulltext
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