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Hypothermia Device
Hypothermia Treatment for Heart Attack (CHIPAHA Trial)
N/A
Waitlist Available
Research Sponsored by Life Recovery Systems
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age ≥ 18 years
Eligible for PCI
Must not have
Cardiogenic shock (systolic blood pressure (SBP) < 80 mmHg for > 30 minutes or SBP < 100 mmHg on vasopressors or IABP) in the absence of bradycardia or other correctable causes
Severe allergy or contraindication to aspirin, Plavix, heparin, or contrast media which cannot be adequately pre-medicated
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial tests whether it's safe to use a cooling system to sedated heart attack patients before surgery.
Who is the study for?
This trial is for adults over 18 who've had heart attack symptoms for 30 minutes to 6 hours and show certain signs on a heart test. They must fit specific size criteria, agree to the study's terms, and be eligible for a procedure to open blocked arteries. People with recent cardiac arrests or heart attacks, low blood pressure shock states, allergies to cold temperatures or certain drugs, pregnancy, participation in other trials, recent surgeries or bleeding disorders can't join.
What is being tested?
The study tests if patients having a severe type of heart attack can be quickly cooled down using the ThermoSuit System before getting an artery-opening procedure. The goal is to see if this cooling (therapeutic hypothermia) is safe and effective when done right before fixing the blocked arteries.
What are the potential side effects?
Potential side effects may include reactions related to being cooled rapidly such as shivering or discomfort from the cold. There might also be risks associated with sedation needed during the process.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Select...
I am eligible for a heart procedure to improve blood flow.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have had very low blood pressure for more than 30 minutes without a slow heartbeat.
Select...
I have severe allergies to aspirin, Plavix, heparin, or contrast media that can't be managed with medication.
Select...
I have received clot-dissolving medication.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: ThermoSuit-Induced Patient CoolingExperimental Treatment1 Intervention
The Life Recovery Systems ThermoSuit System will be used to cool STEMI patients under conditions of conscious sedation.
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Who is running the clinical trial?
Life Recovery SystemsLead Sponsor
4 Previous Clinical Trials
51 Total Patients Enrolled
Robert J Freedman, M.D.Study ChairLife Recovery Systems
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have a known sensitivity to cold temperatures, such as having Raynaud's disease or cryoglobulinemia.You have a history of blood clotting problems or do not want to receive blood transfusions.I have had a heart attack or cardiac arrest in the last month.I am 18 years old or older.I had surgery less than a week ago.Your body temperature is less than 35°C when you arrive at the Emergency Department.I have had very low blood pressure for more than 30 minutes without a slow heartbeat.My heart attack symptoms lasted between 30 minutes and 6 hours.I am eligible for a heart procedure to improve blood flow.I have severe allergies to aspirin, Plavix, heparin, or contrast media that can't be managed with medication.You are allergic to midazolam, meperidine, buspirone, or magnesium sulfate.You have a specific heart condition where the ST segment on an electrocardiogram is elevated by 1mm or more in two or more nearby leads.I have received clot-dissolving medication.
Research Study Groups:
This trial has the following groups:- Group 1: ThermoSuit-Induced Patient Cooling
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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