Recruiting

Bivalirudin

Sponsor:

Laval University

Code:

NCT01084993

Conditions

Coronary Artery Disease

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Bivalirudin

Heparin

Study Details

Brief summary:

RATIONALE:

Transradial coronary stenting is associated with less risk of access site complications and bleeding compared to femoral approach.

Major bleeding post-PCI is a strong independent predictor of mortality and MACE. Depending of the antithrombotic regimen and access-site used, bleeding related to access-site represents 50-80% of the cases. Whereas transradial approach minimizes the risks of access-site bleeding, it has no impact on non-access site bleeding.

Peri-procedural anemia is also an independent predictor of mortality and MACE.

With femoral approach, bivalirudin compared to heparin ± glycoproteins IIb-IIIa has been associated with a significant reduction in access-site and non-access site related bleeding.

In a post-hoc analysis of patients treated by transradial approach in ACUITY, there was a trend for non-access site bleeding (organ bleeding) with bivalirudin compared to heparin ± glycoproteins IIb-IIIa.

HYPOTHESES:

In patients at high-risk of peri-procedural bleeding, bivalirudin ± glycoproteins IIb-IIIa reduces the risk of bleeding compared to heparin ± glycoproteins IIb-IIIa.

In patients at high-risk of bleeding and undergoing transradial PCI, bivalirudin significantly reduces the incidence of non-access site bleeding and peri-procedural anemia.

Conditions

Coronary Artery Disease

Study ID

NCT01084993

Start date

Mar, 2010

Status verified date

Jan, 2018

Completion date

Jan, 2019

Anticipated

Primary completion date

Sep, 2018

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • At least two of the following additional criteria
  • At least 70 yrs old
  • Female gender
  • Diabetes
  • Creatinine clearance <60mL/min
  • History of gastro-intestinal or other organ bleeding
  • Baseline anemia
  • Current treatment with glycoproteins IIb-IIIa inhibitors

Exclusion Criteria:

  • Intolerance or allergy to ASA, clopidogrel or ticlopidine precluding treatment for 12 months
  • Concurrent participation in other investigational study
  • Femoral sheath (artery)

Study Design

Enrollment

2000 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: Bivalirudin

Standard practice: 0.75mg/kg + infusion 1.75mg/kg/h

active comparator: Heparin

70 U/kg or standard practice

Interventions

Bivalirudin

Standard practice: 0.75mg/kg + infusion 1.75mg/kg/h

Heparin

70 U/kg

Primary outcome measure

  • Major bleeding and Mace [ Time Frame: 24h post-PCI and Discharge ]

Central Contacts and Locations

Central contacts

Locations

Quebec Heart-Lung Institute

Recruiting

Quebec, Canada, G1V 4G5

Contacts

Principal Investigator:

Olivier F Bertrand, MD, PhD

More Information

Sponsor

Laval University

Last update posted

Jan 31, 2018

Last verified

Jan, 2018

Keywords

  • Coronary artery stenting, transradial, intracoronary

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Laval University on 2018-01-31.