Trials / Terminated
TerminatedNCT00128791
Nitroprusside for Prevention of no-Reflow in Primary Angioplasty
Intracoronary Nitroprusside for the Prevention of the No-Reflow Phenomenon Following Primary Percutaneous Coronary Intervention in Acute Myocardial Infarction. A Randomized, Double Blind, Placebo-Controlled Clinical Trial
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 100 (planned)
- Sponsor
- Soroka University Medical Center · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
In patients admitted with acute myocardial infarction, there is a total occlusion of a coronary artery. Even after emergency catheterization and angioplasty, in some patients, the resumed blood flow is suboptimal and impacts on heart function. The study is aimed at examining whether nitroprusside, an anti-hypertension medication, given directly into the coronary artery, can improve the blood flow after the removal of the obstruction that caused the infarction.
Detailed description
Inadequate myocardial tissue perfusion despite successful relief of the culprit occlusion and restoration of epicardial coronary flow for ST-segment elevation acute myocardial infarction (STEMI) results in poor outcome. The investigators hypothesized that nitroprusside (NTP) injected intracoronary immediately before angioplasty might prevent no-reflow and improve vessel flow and myocardial perfusion.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nitroprusside |
Timeline
- Start date
- 2003-01-01
- Completion
- 2005-04-01
- First posted
- 2005-08-10
- Last updated
- 2007-05-25
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT00128791. Inclusion in this directory is not an endorsement.