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Completed

NCT Number: NCT05077657

Safe Surveillance of PCI Under Mechanical Circulatory Support With the Saranas Early Bird Bleed Monitoring System

The objective of this study is to establish the safety of complex high-risk Percutaneous Coronary Intervention (PCI) using Mechanical Circulatory Support (MCS) and surveillance with the Saranas Early Bird Bleed Monitoring System (EBBMS).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

St. Joseph Hospital / Arizona Heart, Phoenix, Arizona, United States

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About this study

To demonstrate that patients undergoing complex high-risk PCI using MCS and surveillance with the Saranas Early Bird Bleed Monitoring System will have relative incidence rate reduction of access site related BARC type III or V bleeding. An optimal outcome will show a a reduction in access-site related bleeding rate when using MCS with the Saranas EBBMS in high-risk PCI patients compared to historical incidence rate.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ≥18 years of age
  • Planned complex high-risk PCI using MCS with Impella from a femoral access and use of Saranas Early Bird Bleed Monitoring System
  • The study patient has been informed of the nature of the study, agrees to its provisions, and has provided written informed consent as approved by the institutional review board of the respective clinical site.

Exclusion criteria

  • Absolute contraindications or allergy to iodinated contrast that cannot be adequately treated with pre-medication
  • Active bleeding
  • Incapacity to access safely femoral artery or femoral vein
  • Significant femoral, iliac, abdominal, or thoracic aortic disease which precludes placement of MCS
  • Anemia (Hgb <9 g/dL), thrombocytopenia (Plt <50,000 cell/mL), history of bleeding diathesis or coagulopathy, or hypercoagulable states
  • Active infection not controlled with antibiotic therapy
  • Currently pregnant or women of child-bearing potential without documented negative pregnancy test
  • Estimated life expectancy < 24 hours
  • Patient is in cardiogenic shock at the time of enrollment

Treatment and study plan

Early Bird® Bleed Monitoring System

Device

The Early Bird Bleed Monitoring System is used in endovascular procedures to monitor and detect internal bleeding complications in real-time.

Impella®

Device

Impella is an FDA-approved percutaneous heart pump indicated for patients with severe coronary artery disease requiring high-risk PCI.

Primary outcomes

  1. Incidence of access site related BARC type III or V bleeding

    Time frame: Within 24 hours

Secondary outcomes

  1. Incidence of activation of each Saranas Early Bird level 1, 2 and 3 indicator

    Time frame: Within 24 hours

  2. Incidence of all BARC type III or V bleeding

    Time frame: Within 24 hours

Other outcomes

  1. Access site related bleeding complications

    Time frame: Within 24 hours

    Safety Endpoint

  2. Access site related vascular complications

    Time frame: Within 24 hours

    Safety Endpoint

  3. Access site related blood transfusions

    Time frame: Within 24 hours

    Safety Endpoint

  4. Non-access site related bleeding complications

    Time frame: Within 24 hours

    Safety Endpoint

  5. Non-access site related vascular complications

    Time frame: Within 24 hours

    Safety Endpoint

  6. Non-access site related blood transfusions

    Time frame: Within 24 hours

    Safety Endpoint

  7. All blood transfusions

    Time frame: Within 24 hours

    Safety Endpoint

  8. Hemoglobin drop

    Time frame: Within 24 hours

    Safety Endpoint

  9. Death

    Time frame: Within 24 hours

    Safety Endpoint

  10. Device and procedure-related adverse events

    Time frame: Within 24 hours

    Safety Endpoint

  11. Serious adverse events

    Time frame: Within 24 hours

    Safety Endpoint

  12. Serious adverse device effects

    Time frame: Within 24 hours

    Safety Endpoint

Sponsors and collaborators

Lead sponsor

Saranas, Inc.

Industry

Collaborators

  • Cardiovascular Research Foundation, New York
  • Proxima CRO

Registry information

Acronym: SAFE-MCS

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Oct 14, 2021
Registry last updated
Feb 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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