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Clinical Trials/NCT02152904
NCT02152904CompletedNot Applicable

Risk Factors of Rebleeding After Peptic Ulcer Bleeding: a Nationwide Cohort Study

Joon Sung Kim1 site in 1 country892 target enrollmentStarted: April 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
892
Locations
1
Primary Endpoint
Rebleeding rate of peptic ulcer bleeding

Study Overview

Brief Summary

The purpose of the investigators study is to investigate the factors associated with rebleeding in patients with peptic ulcer bleeding.

Detailed Description

The investigators are performing a nationwide population based cohort study to investigate the factors associated with rebleeding in patients with peptic ulcer bleeding. The results of the investigators study should give us information about patients who are at high risk of rebleeindg and enable us to manage these patients appropriately.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
20 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients diagnosed with peptic ulcer bleeding by endoscopy
  • Patients who consent to be enrolled in the study

Exclusion Criteria

  • Patients who refuse to be enrolled in the study

Outcomes

Primary Outcomes

Rebleeding rate of peptic ulcer bleeding

Time Frame: 1 year

The rebleeding rate of patients diagnosed with peptic ulcer ble4eding

Secondary Outcomes

  • Mortality rates of peptic ulcer bleeding(30 days)

Investigators

Sponsor
Joon Sung Kim
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Joon Sung Kim

Clinical assistant proffessor, Department of Internal medicine, Incheon St. Mary's Hospital

Incheon St.Mary's Hospital

Study Sites (1)

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