Trials / Terminated
TerminatedNCT00320229
Half-Dose Intracoronary Abciximab Bolus Improves the Mortality Outcome Compared to Standard Intravenous Regimen
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 84 (planned)
- Sponsor
- Azienda Sanitaria Ospedaliera · Academic / Other
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Not accepted
Summary
The aim of our study was to demonstrate that, during a percutaneous coronary intervention, even smaller amounts of abciximab than standard dose, injected locally, could achieve a rapid thrombus resolution and clinical improvement without concomitant differences in hemorrhagic complications
Detailed description
Patients both with acute myocardial infarction and unstable angina are prone to extensive intracoronary thrombosis, leading to acute deterioration during percutaneous coronary intervention or thrombosis of the device despite therapy. Intracoronary use of abciximab has reported favourable results. We randomly assigned 84 patients to intracoronary half abciximab bolus (group A) and to standard regimen (group B).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | abciximab |
Timeline
- Start date
- 2004-12-01
- Completion
- 2005-07-01
- First posted
- 2006-05-03
- Last updated
- 2006-05-16
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT00320229. Inclusion in this directory is not an endorsement.