Evaluation of the prevalence of Osler disease (hereditary hemorrhagic telangiectasia) in patients with gastrointestinal telangiectasia

Evaluation of the prevalence of Osler disease (hereditary hemorrhagic telangiectasia) in patients with gastrointestinal telangiectasia - Evaluation of the prevalence of Osler disease

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000026703

Enrollment

6000

Registered

2017-04-01

Start date

2017-04-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Gastrointestinal telangiectasia

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Subjects who undergo endoscopic examination at our hospital 2) Subjects who are diagnosed with gastrointestinal telangiectasia at endoscpy

Exclusion criteria

Exclusion criteria: Subjects who are judged inadequate for this research

Design outcomes

Primary

Measure	Time frame
Definite diagnosis of Osler disease	—

Secondary

Measure	Time frame
Endoscopic characteristics of gastrointestinal telangiectasia, Clinical background in patients with gastrointestinal telangiectasia, including age, gender, primary disease, administrating drug, symptom, laboratory findings	—

Countries

Japan

Contacts

Public ContactNorihisa Ishimura

Shimane University School of Medicine Department of Internal Medicine II

ishimura@med.shimane-u.ac.jp0853-20-2190

Outcome results