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The Effects of IABP Prior to Revascularization on Mortality of ACS Patients Complicated With Cardiogenic Shock

Primary Purpose

Cardiogenic Shock

Status
Unknown status
Phase
Not Applicable
Locations
Indonesia
Study Type
Interventional
Intervention
Intra Aortic Balloon Pump
Sponsored by
Indonesia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiogenic Shock focused on measuring IABP, Cardiogenic Shock, Myocardial Infarction

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age greater than 18 years old
  • Myocardial infarction patients complicated with shock
  • Willing to enroll in the study (signed consent)

Exclusion Criteria:

  • Age greater than 80 years old
  • Heart and lung resuscitation for more than 30 minutes
  • Cardiogenic shock onset >12 hours (if known) or >18 hours (if not known/patient presented in emergency department already with shock)
  • Mechanical complication of myocardial infarction
  • Moderate and severe aorta regurgitation
  • Peripheral artery disease making IABP unfeasible
  • Patients not receiving revascularization by percutaneous coronary intervention
  • Patients who died before IABP insertion
  • Care termination requested by family

Sites / Locations

  • National Cradiovascular Center Harapan Kita HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Intra Aortic Balloon Pump

Arm Description

Group of patients not receiving IABP

Group of patients receiving Intra Aortic Balloon Pump prior to revascularization

Outcomes

Primary Outcome Measures

30-day-Mortality
Mortality of patients 30 day after hospitalization

Secondary Outcome Measures

Full Information

First Posted
August 15, 2018
Last Updated
February 26, 2019
Sponsor
Indonesia University
Collaborators
National Cardiovascular Center Harapan Kita Hospital Indonesia
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1. Study Identification

Unique Protocol Identification Number
NCT03635840
Brief Title
The Effects of IABP Prior to Revascularization on Mortality of ACS Patients Complicated With Cardiogenic Shock
Official Title
The Effects of Intra Aortic Balloon Pump Prior to Revascularization on Mortality of Patients With Acute Coronary Syndrome Complicated With Cardiogenic Shock
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 4, 2018 (Actual)
Primary Completion Date
December 4, 2019 (Anticipated)
Study Completion Date
December 4, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indonesia University
Collaborators
National Cardiovascular Center Harapan Kita Hospital Indonesia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Prevalence of cardiogenic shock in acute coronary syndrome patients is reported at about 5-8% with high fatality. Revascularization approach has already known as the standard of care, but the usage of intra-aortic balloon pump (IABP) as mechanical circulatory support is still a controversy. IABP SHOCK II trial revealed that short-term mortality did not improved by IABP but there are several essential variabels related to mortality that are not considered in the study which are IABP initiation time and weaning protocol.This study aim to evalute the effect of IABP prior to revascularization on mortality of patients with myocardial infarction complicated with shock. 92 subjects will be enrolled in this randomized controlled trial into two groups, with and without IABP. IABP group will be receiving the intervention prior to revascularization. The primary outcomes to be sought are in-hospital and 30-day mortality after revascularization. IABP effects measured by various indicators such as Global Longitudinal Strain by echocardiography on the 1st and 3rd day, NTproBNP and ST2 level on the 1st, 3rd and 5th day, effective lactate clearance and ureum creatinine level on the 1st and 3rd day and will be compared between two groups. Continous variabel will be presented in mean ± deviation standard or median, and analized with Student's t test or Mann-Whitney U test as appropriate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiogenic Shock
Keywords
IABP, Cardiogenic Shock, Myocardial Infarction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
92 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Group of patients not receiving IABP
Arm Title
Intra Aortic Balloon Pump
Arm Type
Experimental
Arm Description
Group of patients receiving Intra Aortic Balloon Pump prior to revascularization
Intervention Type
Device
Intervention Name(s)
Intra Aortic Balloon Pump
Other Intervention Name(s)
IABP
Intervention Description
Intra Aortic Balloon Pump (IABP) is a circulatory mechanical support device, placed in descending aorta, distally from left subclavian artery and proximally from renal artery. IABP works with counterpulsation concept, synchronized with heart cycle. It is indicated as supportive therapy for patients undergoing revascularization, cardiogenic shock and mechanical complication. Balloon dilatation during dyastolic phase increasing dyastolic pressure in aorta, improving coronary vascularization and myocardial oxygen supply. In systolic phase, the balloon deflates, reducing the left ventricle afterload hence decreasing myocardial oxygen demand.
Primary Outcome Measure Information:
Title
30-day-Mortality
Description
Mortality of patients 30 day after hospitalization
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age greater than 18 years old Myocardial infarction patients complicated with shock Willing to enroll in the study (signed consent) Exclusion Criteria: Age greater than 80 years old Heart and lung resuscitation for more than 30 minutes Cardiogenic shock onset >12 hours (if known) or >18 hours (if not known/patient presented in emergency department already with shock) Mechanical complication of myocardial infarction Moderate and severe aorta regurgitation Peripheral artery disease making IABP unfeasible Patients not receiving revascularization by percutaneous coronary intervention Patients who died before IABP insertion Care termination requested by family
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dafsah Juzar, MD
Phone
+621-5684093
Ext
1265
Email
djuzar@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Arum Suryandari, MD
Phone
+621-5684093
Ext
1265
Email
arumramadhyan@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dafsah Juzar, MD
Organizational Affiliation
National Cardiovascular Center Harapan Kita Hospital Indonesia
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Cradiovascular Center Harapan Kita Hospital
City
Jakarta
ZIP/Postal Code
11420
Country
Indonesia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dafsah Juzar, MD
Phone
+621-5684093
Ext
1265
Email
djuzar@gmail.com
First Name & Middle Initial & Last Name & Degree
Gloria Kartika, MD
Phone
+621-5684093
Ext
1265
Email
gloria_kartika@yahoo.com
First Name & Middle Initial & Last Name & Degree
Dafsah Juzar, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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The Effects of IABP Prior to Revascularization on Mortality of ACS Patients Complicated With Cardiogenic Shock

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