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How Effective Are Antithrombotic Therapies in Primary Percutaneous Coronary Intervention (HEAT-PPCI)

Primary Purpose

Acute ST Elevation Myocardial Infarction

Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
unfractionated heparin
Bivalirudin
Sponsored by
Liverpool Heart and Chest Hospital NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute ST Elevation Myocardial Infarction focused on measuring ST elevation myocardial infarction, Primary percutaneous coronary intervention, Unfractionated heparin, Bivalirudin, primary angioplasty

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients presenting with a suspected myocardial infarction event with PPCI as the proposed index reperfusion strategy will be included in the trial

Exclusion Criteria:

  • ≤ 18 years of age
  • Known intolerance, hypersensitivity or contraindication to any trial medication
  • Active bleeding at presentation
  • Artificial ventilation, reduced conscious level or other factors precluding the administration of oral antiplatelet therapy
  • Previous enrolment in this trial

Sites / Locations

  • Liverpool Heart and Chest Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Unfractionated heparin

bivalirudin

Arm Description

70 units/kg body weight intravenous

intravenous bolus of 0.75 mg/kg followed by infusion of 1.75 mg/kg per hour

Outcomes

Primary Outcome Measures

Major Adverse Cardiac Events (MACE) in Terms of the Incidence of All Cause Mortality, Cerebrovascular Accident, Re-infarction and Additional Unplanned Target Lesion Revascularization
Type 3-5 Bleeding According to BARC (Bleeding Academic Research Consortium)Definition

Secondary Outcome Measures

CKMB Release Following Index Revascularisation Measured With a Single Estimation 12-18 Hours After the Procedure
Minor Bleeding: Type 2 Bleeding According to BARC (Bleeding Academic Research Consortium) Definition
Stent Thrombosis Rate (ARC Definite or Probable)
For Illustration, and to Allow Comparison With Existing Trials the Rate of Net Adverse Clinical Events (NACE), Combining the Primary Safety and Efficacy Outcomes
All Cause Mortality
Development of Thrombocytopenia
Door-to-first Device Time

Full Information

First Posted
January 24, 2012
Last Updated
April 24, 2015
Sponsor
Liverpool Heart and Chest Hospital NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT01519518
Brief Title
How Effective Are Antithrombotic Therapies in Primary Percutaneous Coronary Intervention
Acronym
HEAT-PPCI
Official Title
A Randomised Controlled Trial to Compare Unfractionated Heparin Versus Bivalirudin in the Treatment of Patients With a Clinical Diagnosis of ST-Segment Elevation Myocardial Infarction Events - For Planned Management With Primary PCI
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
February 2012 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Liverpool Heart and Chest Hospital NHS Foundation Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare unfractionated heparin (UFH) and bivalirudin in the performance and subsequent outcomes of Primary percutaneous coronary intervention. This will be a pragmatic trial. Interventional procedures will be performed to reflect current and evolving standards, including predominant radial access. All patients will be treated with routine oral anti-platelet therapy pre-procedure. GP IIb/IIIa inhibitors will be reserved for 'bail out' treatment only.
Detailed Description
HEAT-PPCI is a single-centre prospective, dual-arm, open-label, randomised controlled trial comparing two antithrombotic agents in patients undergoing PPCI. All patients presenting to the PPCI service at Liverpool Heart and Chest Hospital will be assessed for trial eligibility. The patients will be allocated by randomisation in equal proportions to the two treatment groups receiving UFH (70 units/kg prior to the procedure) or bivalirudin (bolus of 0.75 mg/kg prior to the start of the intervention, followed by an infusion of 1.75 mg/kg per hour for the duration of the procedure). Pre-Specified Subgroup Analyses Subgroup analyses looking at the impact of access site comparing radial versus femoral route Assessment of the outcomes in diabetic patients receiving oral hypoglycaemic or insulin therapy versus all other patients Comparing the outcomes in patients < or ≥ 75 years of age Type of p2y12 receptor inhibiting antiplatelet agent (Examples: clopidogrel, prasugrel, ticagrelor) Patients with impaired LV function versus normal LV function Patients managed with actual or attempted primary PCI versus no immediate PCI procedure attempted PLATELET FUNCTION SUBSTUDY A substudy will be performed to assess indices of coagulation and platelet function studies comparing the impact of heparin or bivalirudin therapy on coagulation status at the end of the PPCI procedure. This study will be performed on all patients treated between the hours of 0800 and 1600, Monday to Friday. A single blood sample taken at the time of general blood sampling for routine clinical screening will be analysed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute ST Elevation Myocardial Infarction
Keywords
ST elevation myocardial infarction, Primary percutaneous coronary intervention, Unfractionated heparin, Bivalirudin, primary angioplasty

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1829 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Unfractionated heparin
Arm Type
Active Comparator
Arm Description
70 units/kg body weight intravenous
Arm Title
bivalirudin
Arm Type
Active Comparator
Arm Description
intravenous bolus of 0.75 mg/kg followed by infusion of 1.75 mg/kg per hour
Intervention Type
Drug
Intervention Name(s)
unfractionated heparin
Other Intervention Name(s)
UFH
Intervention Description
70 units/kg body weight intravenous
Intervention Type
Drug
Intervention Name(s)
Bivalirudin
Other Intervention Name(s)
Angiox
Intervention Description
intravenous bolus of 0.75 mg/kg followed by infusion of 1.75 mg/kg per hour
Primary Outcome Measure Information:
Title
Major Adverse Cardiac Events (MACE) in Terms of the Incidence of All Cause Mortality, Cerebrovascular Accident, Re-infarction and Additional Unplanned Target Lesion Revascularization
Time Frame
28 days
Title
Type 3-5 Bleeding According to BARC (Bleeding Academic Research Consortium)Definition
Time Frame
28 days
Secondary Outcome Measure Information:
Title
CKMB Release Following Index Revascularisation Measured With a Single Estimation 12-18 Hours After the Procedure
Time Frame
28 days
Title
Minor Bleeding: Type 2 Bleeding According to BARC (Bleeding Academic Research Consortium) Definition
Time Frame
28 days
Title
Stent Thrombosis Rate (ARC Definite or Probable)
Time Frame
28 days
Title
For Illustration, and to Allow Comparison With Existing Trials the Rate of Net Adverse Clinical Events (NACE), Combining the Primary Safety and Efficacy Outcomes
Time Frame
28 days
Title
All Cause Mortality
Time Frame
1 year
Title
Development of Thrombocytopenia
Time Frame
28 days
Title
Door-to-first Device Time
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients presenting with a suspected myocardial infarction event with PPCI as the proposed index reperfusion strategy will be included in the trial Exclusion Criteria: ≤ 18 years of age Known intolerance, hypersensitivity or contraindication to any trial medication Active bleeding at presentation Artificial ventilation, reduced conscious level or other factors precluding the administration of oral antiplatelet therapy Previous enrolment in this trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rod Stables, MA DM FRCP
Organizational Affiliation
Liverpool Heart and Chest Hospital, Liverpool, UK
Official's Role
Principal Investigator
Facility Information:
Facility Name
Liverpool Heart and Chest Hospital
City
Liverpool
State/Province
Merseyside
ZIP/Postal Code
L14 3PE
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
25002178
Citation
Shahzad A, Kemp I, Mars C, Wilson K, Roome C, Cooper R, Andron M, Appleby C, Fisher M, Khand A, Kunadian B, Mills JD, Morris JL, Morrison WL, Munir S, Palmer ND, Perry RA, Ramsdale DR, Velavan P, Stables RH; HEAT-PPCI trial investigators. Unfractionated heparin versus bivalirudin in primary percutaneous coronary intervention (HEAT-PPCI): an open-label, single centre, randomised controlled trial. Lancet. 2014 Nov 22;384(9957):1849-1858. doi: 10.1016/S0140-6736(14)60924-7. Epub 2014 Jul 4. Erratum In: Lancet. 2014 Nov 22;384(9957):1848.
Results Reference
derived
PubMed Identifier
24219045
Citation
Malik N, Gershlick AH. The clinical and economic impact of bivalirudin for percutaneous coronary intervention. Expert Rev Pharmacoecon Outcomes Res. 2013 Dec;13(6):699-706. doi: 10.1586/14737167.2013.844650.
Results Reference
derived

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How Effective Are Antithrombotic Therapies in Primary Percutaneous Coronary Intervention

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