Status:

UNKNOWN

Lucid Registry Study

Lead Sponsor:

Lucid Diagnostics, Inc.

Conditions:

Barrett Esophagus

Esophageal Adenocarcinoma

Eligibility:

All Genders

12+ years

Brief Summary

This is a multicenter, prospective, observational study designed to capture a limited set of data consisting of diagnostic test results and clinical management information on subjects who undergo EC/E...

Eligibility Criteria

Inclusion

  • Males and Females who have provided informed consent for prospective registry participation
  • Subject in whom the clinical decision has been made to screen for BE/EAC using EsoGuard testing on samples collected with EsoCheck

Exclusion

  • Inability to provide written informed consent
  • Subjects who fall outside the eligible population defined by the EsoCheck device Instructions For Use (IFU)

Key Trial Info

Start Date :

April 11 2023

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

June 1 2024

Estimated Enrollment :

500 Patients enrolled

Trial Details

Trial ID

NCT05965999

Start Date

April 11 2023

End Date

June 1 2024

Last Update

July 28 2023

Active Locations (1)

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1

LUCID DX

Lake Forest, California, United States, 92630