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A Nationwide Study of Esophageal Bleeding and Strictures Caused by Reflux Esophagitis

A Nationwide Study of Esophageal Bleeding and Strictures Caused by Reflux Esophagitis - Study for the COmplication of Reflux Esophagitis (SCORE)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000014157
Enrollment
5300
Registered
2014-10-01
Start date
2014-10-01
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

Reflux esophagitis (RE)

Interventions

None listed

Sponsors

Society for GERD
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients with LA Grade A or greater RE confirmed during the study period by upper gastrointestinal endoscopy performed for a reason unrelated to a health examination. (2) Outpatient or hospitalized men and women at least 50 years of age. (3) Patients who have personally or via a legally acceptable representative given written consent.

Exclusion criteria

Exclusion criteria: (1) Patients with RE occurring subsequent to upper gastrointestinal tract resection, endoscopic treatment of the upper gastrointestinal tract, or gastrostomy. (2) Patients whom the investigators find ineligible for participation in the study for any reason.

Design outcomes

Primary

MeasureTime frame
Clinical characteristics of RE patients with RE-induced bleeding or strictures (deformation).

Countries

Japan

Contacts

Public ContactNoriaki Manabe

Kawasaki Medical School Division of Endoscopy and Ultrasonography

n_manabe@med.kawasaki-m.ac.jp086-462-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026