A prospective observational study about discontinuation or continuation of the antithrombotic drug at the time of the upper non-varix gastrointestinal tract bleeding

A prospective observational study about discontinuation or continuation of the antithrombotic drug at the time of the upper non-varix gastrointestinal tract bleeding - A prospective observational study about discontinuation or continuation of the antithrombotic drug at the time of the upper non-varix gastrointestinal tract bleeding

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000016381

Enrollment

150

Registered

2015-01-29

Start date

2015-01-29

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

non-varix upper gastrointestinal tract bleeding

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Subjects obtained written informed consent 2) Subjects taking antithrombotic drug for more than 1 month 3) Subjects who had a diagnosis of upper gastrointestinal tract bleeding with esophagogastroduodenoscopy

Exclusion criteria

Exclusion criteria: bleeding from varix

Design outcomes

Primary

Measure	Time frame
Re-bleeding rate	—

Secondary

Measure	Time frame
number of times of hemostasis, fast period, length of stay, quantity of total blood transfusion	—

Countries

Japan

Contacts

Public ContactJun Takada

Gifu University Hospital Gastroenterology

jtakada-gifu@umin.ac.jp058-230-6308

Outcome results