CHEETAH:A Prospective Multicenter Study to Evaluate the Safety and Performance of the CAT RX Aspiration Catheter in Patients with a High Thrombus Burden Acute Coronary Vessel Occlusion

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Coronary Vessel Occlusion
  • Age: Between 18 - 120 Years
  • Gender: Male or Female
  • Other Inclusion Criteria:
    1. Subjects presents to treating facility within 12 hours of symptom onset
    2. Subjects has high thrombus burden at coronary angiography, defined as TIMI thrombus grade 4 or 5 by physician visual estimate after the guidewire crosses the target lesion
    3. Subjects with frontline treatment with the Indigo® Aspiration System using the CAT RX Aspiration Catheter, prior to standard of care PCI
    4. Subjects who has target lesion is located in a native coronary artery
    5. Informed consent is obtained from either patient or legally authorized representative (LAR)

You may not be eligible for this study if the following are true:

    1. Subjects with a new onset of stroke symptoms and NIHSS > 2, prior to index procedure
    2. Subjects who are treated with fibrinolytic therapy for index coronary vessel occlusion
    3. Subjects who has life expectancy less than 6 months due to any comorbidities
    4. Subjects who are unwilling or unable to comply with protocol follow up schedule and/or based on the Investigator’s judgment the patient is not a good study candidate
    5. Subjects participating in another investigational drug or device study that may confound the results of this study.
    6. Subjects who are pregnant

If you are registered as a volunteer, please login to the dashboard to send referrals.

Contact the research team to learn more about this study.

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.