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NCT06030180: PR-0410

CLUE: CLinical Utility Study of EsoGuard

Completed NA Last updated 27 June 2025
What this trial tests

NA trial testing EsoGuard in Barrett Esophagus in 566 participants. Completed in 13 December 2024.

Timeline
23 February 2023
Primary endpoint
13 December 2024
13 December 2024

Quick facts

Lead sponsorLucid Diagnostics, Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment566
Start date23 February 2023
Primary completion13 December 2024
Estimated completion13 December 2024
Sites8 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Lucid Diagnostics, Inc.

Who can join

Adults 12 to 99, any sex, with Barrett Esophagus or Barretts Esophagus With Dysplasia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Utilize real-world data from the commercial use of EsoGuard testing on samples collected with EsoCheck (EC/EG) to evaluate the impact of EsoGuard results on health care provider's decision for endoscopy referral. Assess patient compliance with recommendations for upper endoscopy, and relationship of compliance to positive EsoGuard results.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Real-World Clinical Utility of a Methylated DNA Biomarker Assay on Samples Collected with a Swallowable Capsule-Balloon for Detection of Barrett's Esophagus (BE).
    Lister D, Fine A, Maheshwari S, Bradley PS, et al · · 2024 · cited 2× · PMID 39768931 · DOI 10.3390/medicina60122052

Verify or expand the search:

Other trials of EsoGuard

Trials testing the same drug.

Other recruiting trials for Barrett Esophagus

Currently open trials in the same condition.

Other Lucid Diagnostics, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06030180.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing