Predisposing genetic risk factors for Barrett*s Esophagus

Predisposing genetic risk factors for Barrett*s Esophagus - GWAS Barrett*s disease

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON39802

Enrollment

600

Registered

2013-05-22

Start date

2012-11-15

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

Barretts esophagus cell abnormality in the lower esophagus

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with Barrett*s disease

Exclusion criteria

Exclusion criteria: Patients without histological confirmation of BE

Design outcomes

Primary

Measure	Time frame
Primary endpoint: regions on human genome that are associated with BE.	—

Secondary

Measure	Time frame
Secondary endpoints are: BE length, complication of BE (dysplasia, ulcer, stricture or EAC), presence of esophagitis and hiatal hernia, patients* BMI, medication and cardiac history	—

Countries

Netherlands

Outcome results