Efficacy of Endovascular Catheter Cooling Combined With Cold Saline for the Treatment of Acute Myocardial Infarction

Myocardial Infarction Clinical Trial

— CHILL-MI  

Official title:

Rapid Endovascular Catheter Core Cooling Combined With Cold Saline as an Adjunct to Percutaneous Coronary Intervention For the Treatment of Acute Myocardial Infarction

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01379261
• Other study ID #: CHILL-MI
• Status: Completed
• Phase: Phase 2/Phase 3
• First received: June 21, 2011
• Last updated: November 5, 2014
• Start date: June 2011
• Est. completion date: November 2013

Study information

• Verified date: November 2014
• Source: Region Skane
• Contact: n/a
• Is FDA regulated: No
• Health authority: Sweden: Regional Ethical Review Board
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether treatment of patients suffering from ST-elevation myocardial infarction (STEMI) with 1-2 liters of cold saline and central venous catheter cooling with Philips InnerCool RTx Endovascular System prior to percutaneous coronary intervention (PCI) result in a reduction in infarct size.

Description:

Acute myocardial infarction (AMI) is the leading cause of mortality in the western world today. Although reperfusion of the ischemic myocardium is a prerequisite for myocardial salvage, it has been described that the reperfusion in itself may cause additional damage to the myocardium (reperfusion injury). In the safety & feasibility trial RAPID MI-ICE we demonstrated that treatment of patients suffering from STEMI with 1-2 liters of cold saline and central venous catheter cooling with Philips InnerCool RTx Endovascular System prior to PCI was feasible, safe and resulted in a 38% reduction in infarct size/myocardium at risk. The aim of the present study is to confirm this finding in a larger multicenter trial.

The study is a randomized, controlled, evaluator blinded, multicenter trial enrolling 120 patients at ten sites.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 120
• Est. completion date: November 2013
• Est. primary completion date: September 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 79 Years

Eligibility

Inclusion Criteria:

1. Clinical symptoms and signs of myocardial infarction and have a 12-lead ECG providing evidence of an ongoing acute myocardial infarction, involving a large area of myocardium, as defined by the following ECG criteria. The ECG changes should be present upon arrival to the cath lab:

1. Anterior infarct: ST-segment elevation >0.2mV measured 0.08 sec after the J point in 2 or more anatomically contiguous precordial leads, V1 through V4; and/or >0.2mV in lead V5 V6.

2. Inferior infarct: ST elevation >0.2mV measured 0.08 sec after the J point in 2 or more anatomically contiguous inferior leads, coupled with ST depression in 2 contiguous anterior leads for a total ST deviation (inferior ST elevation plus anterior ST depression) of >0.8mV.

2. Present to the study PCI lab within six (6) hours of the onset of acute cardiac ischemic signs or symptoms (such as chest pain or pressure, arm or jaw pain, dyspnea, nausea/vomiting, or syncope).

3. Be a candidate for PCI and have PCI planned as the immediate intervention.

4. Be willing and able to comply with study procedures, including returning for the MRI scan at 4 ±2 days and be available for additional follow up Subject understands study procedures and agrees to participate in the study by giving written informed consent.

5. Be in Killips Class I.

Exclusion Criteria:

1. Age less than eighteen (<18) years of age

2. Age greater than or equal to eighty (80) years of age

3. Are pregnant.

4. Having an aortic dissection

5. History of a prior large myocardial infarct or an infarct in the same segment that is currently affected.

6. Acute administration of a thrombolytic agent for the qualifying MI

7. Clinical suspicion of a non-thrombotic (e.g., pericarditis, vasospasm, takotsubo, illicit drug use) cause for ST-segment elevation as determined by the investigator

8. If (during the screening process) the determination is made by site-study personnel that initiation of cooling prior to diagnostic coronary angiography is technically not feasible for any reason (should the patient be randomized to the Hypothermia Arm), the prospective subject should not be enrolled.

9. Known risk for heparin induced thrombocytopenia (HIT)

10. Require an immediate surgical or procedural intervention other than PCI (e.g. CABG)

11. Present in cardiogenic shock or with end-stage cardiomyopathy

12. Have undergone at least ten (10) minutes of cardiopulmonary resuscitation (CPR) prior to presentation to the PCI facility

13. History of surgical coronary artery revascularization (e.g. CABG)

14. Active bleeding, coagulopathy, or other contraindication to the placement of a heparin-coated 14F central venous catheter via a 14F femoral venous introducer sheath (e.g., known history of heparin induced thrombocytopenia, or IVC filter)

15. Contraindications to hypothermia

16. Personal or familial history of malignant hyperthermia

17. Known end-stage renal disease (ESRD; e.g., on dialysis, or status-post renal transplant), known severe hepatic failure (e.g., cirrhosis, or acute hepatitis), or any other contraindication to receiving meperidine (such as use of MAO inhibitors within previous 14 days, history of seizures, history of hypersensitivity to meperidine, etc.).

18. Serious concurrant medical condition likely to result in death during the next 12 months. Any other acute or chronic condition which the Investigator believes will unacceptably increase the risk of study participation or interfere with study procedures and assessments.

19. Contraindication to MRI (e.g., cardiac pacemaker, ICD, nerve stimulator, brain aneurysm clips, cochlear implants, claustrophobia)

20. Deemed unsuitable by the investigators to participate in the study.

21. Active or recent (within 1 month prior to study enrollment) participation in another investigational clinical research study.

22. Enrollment in or planned to be enrolled in another study of AMI therapy

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Anterior Wall Myocardial Infarction
• Infarction
• Inferior Wall Myocardial Infarction
• Myocardial Infarction
• Myocardial Reperfusion Injury
• Reperfusion Injury

Intervention

Procedure:
• Cooling
1-2 liters of cold saline and central venous catheter cooling with Philips InnerCool RTx Endovascular System prior to PCI

Locations

Country	Name	City	State
Austria	Graz University Hospital	Graz
Austria	Innsbruck University Hospital	Innsbruck
Austria	Medical University of Vienna	Vienna
Denmark	Aarhus University Hospital	Aarhus
Denmark	Rigshospitalet - Copenhagen University Hospital	Copenhagen
Slovenia	University Medical Centre	Ljubljana
Sweden	Sahlgrenska University Hospital	Gothenburg
Sweden	Skane University Hospital, Lund, Sweden	Lund
Sweden	Karolinska University Hospital	Stockholm
Sweden	Uppsala University Hospital	Uppsala

Sponsors (4)

Lead Sponsor	Collaborator
Region Skane	Lund University, Philips Healthcare, Uppsala University

Countries where clinical trial is conducted

Austria,  Denmark,  Slovenia,  Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Myocardial infarct size (as a percentage of myocardium at risk) assessed by cardiac MRI.		At 4±2 days	No
Secondary	Myocardial infarct size (as a percentage of myocardium at risk) both assessed by cardiac MRI at 4±2 days in the patients who are cooled and achieve a target temperature of < 35 C prior to PCI.		At 4±2 days	No
Secondary	Myocardial infarct size (as a percentage of myocardium at risk) both assessed by cardiac MRI at 4±2 days in patients with an occluded and non-occluded IRA before PCI.		At 4±2 days	No
Secondary	Myocardial infarct size (as a percentage of myocardium at risk) both assessed by cardiac MRI at 4±2 days in the per protocol population who are cooled according to protocol and meet inclusion criteria.		At 4±2 days	No
Secondary	Myocardial infarct size (as a percentage of myocardium at risk) both assessed by cardiac MRI at 4±2 days in patients with anterior or inferior myocardial infarctions separately.		At 4±2 days	No
Secondary	The effect of the hypothermia protocol on the incidence of death.		45±15 days and 6 months.	No
Secondary	Plasma level of high sensitivity Troponin T AUC through 48 hours and peak plasma level of high sensitivity Troponin T within 48 hours after AMI.		48 hours	No
Secondary	ST-segment resolution 1.5 hour after opening the IRA.		1.5 hours	No
Secondary	Coronary blood flow and coronary angiography at the index event estimated by TIMI coronary flow and coronary perfusion grading.		2 hours	No
Secondary	Plasma NT-proBNP levels at day 4±2.		Day 4±2.	Yes
Secondary	Incidence of death at 1, 2, 3, 4 and 5 years.		5 years	No
Secondary	Myocardial infarct size (as a percentage of myocardium at risk) assessed by cardiac MRI at 6±1 months.		6 months	No
Secondary	Incidence of heart failure within 45±15 days.		6 months	Yes
Secondary	Incidence of pulmonary oedema.		1 week	Yes
Secondary	Incidence of infections		1 week	Yes
Secondary	Incidence of bleedings		1 week	Yes
Secondary	The effect of the hypothermia protocol on the incidence of recurrent MI.		6 months	No
Secondary	The effect of the hypothermia protocol on the incidence of emergent stent revascularisation.		6 months	No
Secondary	The effect of the hypothermia protocol on the incidence of any hospitalisation.		6 months	No