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Balloon Pump Assisted Coronary Intervention Study

NCT00910481 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 301

Last updated 2024-08-07

Study results available
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Summary

This study will test the hypothesis that elective use of the Intra-Aortic Balloon Pump (IABP) in patients undergoing high-risk Percutaneous Coronary Intervention (PCI) will reduce the rate of in-hospital major adverse cardiac and cerebrovascular events compared to patients who are managed without planned insertion of IABP.

Conditions

Interventions

DEVICE

Intra-Aortic Balloon Pump

Elective IABP insertion before PCI

Sponsors & Collaborators

  • British Cardiovascular Intervention Society

    lead OTHER

Principal Investigators

  • Divaka Perera, MRCP, MD · Guy's and St Thomas' Hospital NHSFT, London, UK

  • Simon Redwood, FRCP, MD · Guy's and St Thomas' Hospital NHSFT, London, UK

  • Rodney Stables, FRCP, DM · Liverpool Cardiothoracic Centre, Liverpool, UK

  • Martyn Thomas, FRCP, MD · Guy's and St Thomas' Hospital NHSFT, London, UK

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-12-31
Primary Completion
2011-01-31
Completion
2012-12-31

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00910481 on ClinicalTrials.gov