Related trials
ZEST AMI (vs SES), 2009 - zotarolimus ES vs sirolimus ES
TRIANA, 2009 - primary ballon angioplasty vs tenecteplase
NORDISTEMI, 2009 - thrombolysis + angioplasty vs immediate thrombolysis
Juwana, 2009 - sirolimus ES vs paclitaxel ES
ZEST AMI (vs PES), 2009 - zotarolimus ES vs paclitaxel ES
PASEO, 2009 - drug ES vs bare-metal stent
CARESS, 2008 - thrombolysis + angioplasty vs immediate thrombolysis
HORIZONS-AMI Stent, 2008 - paclitaxel ES vs bare-metal stent
MISSION, 2008 - sirolimus ES vs bare-metal stent
DEDICATION, 2008 - drug ES vs bare-metal stent
Díaz de la Llera, 2007 - sirolimus ES vs bare-metal stent
SESAMI, 2007 - sirolimus ES vs bare-metal stent
TYPHOON, 2006 - sirolimus ES vs bare-metal stent
PROSIT, 2006 - sirolimus ES vs paclitaxel ES
HAAMU-STENT, 2006 - paclitaxel ES vs bare-metal stent
PASSION, 2006 - paclitaxel ES vs bare-metal stent
WEST, 2006 - systematic PCI (+stent) vs no systematic PCI
CAPITAL AMI, 2005 - thrombolysis + angioplasty vs immediate thrombolysis
Di Lorenzo et al., 2005 - sirolimus ES vs paclitaxel ES
ZWOLLE 6, 2005 - primary stenting vs ballon angioplasty
CAPITAL AMI, 2005 - systematic PCI (+stent) vs no systematic PCI
senior PAMI, 2005 - primary PCI vs thrombolytic therapy
STOPAMI 3, 2004 - primary stenting vs ballon angioplasty
GRACIA-1, 2004 - systematic PCI (+stent) vs no systematic PCI
MERLIN (Sutton), 2004 - immediate systematic ballon angioplastyte vs no immediate angioplasty
See also:
All acute myocardial infarction clinical trials
All clinical trials of myocardial revascularization
All clinical trials of Prehospital thrombolysis
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Treatments
| Studied treatment |
anistreplase by mobile intensive care unit
|
| Control treatment |
|
| Treatments description |
| Thrombolytic agent |
Anistreplase |
| Time from sympton onset to thrombolysis |
median 131/180 min |
| Provider |
MICU |
|
Patients
| Inclusion criteria |
Age <75 y Chest pain onset <6 h and lasting 30 min to 3h not responding to nitrates ST-segment elevation of >=0.2 mV in 2 or more standard leads or 3 precordial leads |
| Exclusion criteria |
History of severe hypertension, classic contraindications to thrombolysis (not defined) |
Method and design
| Randomized effectives |
57 / 43 (studied vs. control) |
Results
Endpoint
Studied treat. n/N
Control treat. n/N
Graph
RR [95% CI]
All cause death
3 / 57
3 / 43
classic
0,75 [0,16;3,56]
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
|
3 / 57 (5,3%) |
3 / 43 (7,0%) |
0,75 |
[0,16;3,56] |
|
|
|
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
|
| Endpoint |
Events rate |
Absolute risk reduction (ARR) |
| Studied treat. |
Control treat. |
| All cause death |
5,26% |
6,98% |
-17,1‰
|
Reference(s)
-
Castaigne AD, Hervé C, Duval-Moulin AM, Gaillard M, Dubois-Rande JL, Boesch C, Wolf M, Lellouche D, Jan F, Vernant P.
Prehospital use of APSAC: results of a placebo-controlled study..
Am J Cardiol 1989;64:30A-33A; discussion 41A-42A
Pubmed
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Hubmed
| Fulltext
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