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Study of the Risk Factors and Outcomes After Gastrointestinal Bleeding

NCT02514304 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4745

Last updated 2025-07-31

No results posted yet for this study

Summary

The purpose of this multicenter, two component observational and standardized case-control study is to evaluate risk factors of gastrointestinal (GI) bleeding with a prospective 3-month and 12-month follow-up to examine outcomes and their possible causes.

Conditions

Sponsors & Collaborators

  • Heart and Stroke Foundation of Ontario

    collaborator OTHER

  • Bristol-Myers Squibb

    collaborator INDUSTRY

  • Daiichi Sankyo

    collaborator INDUSTRY

  • Population Health Research Institute

    lead OTHER

Principal Investigators

  • John Eikelboom, MD · Population Health Research Institute, McMaster University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-30
Primary Completion
2023-12-15
Completion
2024-12-31

Countries

  • Canada

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02514304 on ClinicalTrials.gov