Skip to content

Anti Ischemic Effects of Abciximab in Angioplasty and Stenting Patients

Anti Ischemic Effects of Abciximab in Angioplasty and Stenting Patients (AIR)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00379418
Acronym
AIR
Enrollment
220
Registered
2006-09-21
Start date
2003-01-31
Completion date
2009-12-31
Last updated
2013-09-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease

Brief summary

AIR STUDY TITLE: Anti-Ischemic effects of Abciximab(Reopro) PATIENT POPULATION: Patients undergoing PCI(an interventional procedure placing a small stent/metallic tube to keep a narrowed artery in your heart open) and either on a stable statin dose or not on a statin. Statin= cholesterol lowering drug(ie, lipitor, zocor). INTERVENTION: Heparin vs. heparin + abciximab during PCI PURPOSE: Measure the effects of abciximab on special healing blood stem cells (EPC's-Endothelial Progenitor Cells), on inflammation, on oxidative stress and on microvascular blood flow. PATIENT ASSESSMENT: 1. 50ccs blood draw on day 1(from sheath), day 2 ,day 7 and day 28. 2. Measurement of blood flow in selected suitable patients 3. 10 minute questionnaire before discharge and on visit on day 28.

Interventions

DRUGAbciximab

Sponsors

Emory University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

1. Have either: * clinical history of anginal symptoms or positive stress test or * in stent restenosis 2. Have an angiographic \>70% coronary artery stenosis that will be treated with coronary angioplasty or stenting procedure 3. For at least four weeks prior to the procedure have been on, no Hmgcoa- reductase inhibitor or a stable statin dose 4. negative pregnancy test 5. are able to give informed consent

Exclusion criteria

1. Coronary intervention within four weeks prior to enrollment. 2. Treatment with abciximab antagonist within four weeks. 3. treatment with thrombolytic therapy within 48 hours 4. MI within 2 months. 5. recent infections 6. general anesthesia within 3 months. 7. renal failure

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026