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Clinical Utility of Methylation-based Prognostic Assay for Barrett's Esophagus

Clinical Utility of Methylation-based Prognostic Assay for Barrett's Esophagus

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05846971
Enrollment
100
Registered
2023-05-06
Start date
2021-01-26
Completion date
2023-12-31
Last updated
2023-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Barrett Esophagus, Esophageal Cancer

Brief summary

Capsulomics has developed a prognostic assay for patients with diagnosed Barrett's esophagus (BE). This study will measure how gastroenterologists make surveillance and treatment management decisions when presented with different clinical and prognostic assay information.

Detailed description

Capsulomics has developed a prognostic assay for patients with diagnosed Barrett's esophagus (BE). This study will measure how gastroenterologists make surveillance and treatment management decisions for virtual patient cases when presented with different clinical and prognostic assay information. The data from this study will be published in a peer-review scientific journal.

Interventions

OTHEREducational materials on validated methylation assay

Educational materials include overall information on the assay including what the test does, how to use the test and report, and performance metrics on the test.

Sponsors

Capsulomics, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Be currently practicing board-certified gastroenterologist practicing in the United States 2. Have practiced (as a board-certified gastroenterologist) for greater than 2 3. Be English-speaking 4. Have ≥ 50 Barrett's esophagus patients under care annually 5. Have Internet access 6. Have no prior experience with the methylation assay test 7. Provide voluntary informed consent to participate in the study.

Exclusion criteria

1. Non-practicing gastroenterologists 2. Less than two years of gastroenterology practice 3. Non-English speaking 4. Does not have access to the internet 5. Does not consent to participate in study

Design outcomes

Primary

MeasureTime frameDescription
Clinical performance change in physician behavior.1 yearChange in the overall and the diagnostic and treatment in patient simulations: difference-in-differences regression analysis between the control and the intervention groups' diagnosis and treatment of risk progression in patients with Barrett's esophagus, as measured by the participants' diagnostic and treatment scores. In each category, participants' care recommendations are evaluated, ranging from 0 to a high potential score of up to 10, where higher scores mean increased intensity in surveillance and treatment, to measure the impact of the methylation assay on care decision making.
The impact of methylation assay on physician confidence in clinical care decision-making.1 yearMeasure the confidence in care decisions based on patient's methylation test result: Once the intervention group is exposed to the intervention, education materials on the methylation assay (a validated molecular test for risk stratifying patients with Barrett's esophagus), the scores are measured, on a scale of 0 to 10 from round 1 (pre-exposure) to round 2 (post-exposure) and observe how the assay impacts confidence in the physician following evidence-based patient care.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026