Observational Study of Outcomes after EchoMark and EchoSure-based Free Flap Monitoring

  • STATUS
    Enrolling By Invitation
  • participants needed
    100
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Updated on 19 February 2024

Summary

The purpose of this study is to evaluate the performance of the EchoMark and EchoSure (both FDA approved devices) as an ultrasound-based method of monitoring the viability of free flaps and patency of at-risk vessels. The implant and ultrasound will be used per IFU. The primary purpose of the study is to collect data on patient outcomes in cases where the surgeon has chosen it as the appropriate method of monitoring.

Details
Condition Free Flap Transfer Malignant Neoplasm
Age 99years or below
Clinical Study Identifier03915717
Last Modified on19 February 2024

Eligibility

If you need help finding a study or have any questions, please contact us at psom-ocr@pobox.upenn.edu

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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