← Eichor
Study identifier: NCT05290857 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Anticoagulation After GI Bleeding Pilot Study and Registry

Condition: GastroIntestinal Bleeding · Anticoagulant-induced Bleeding  ·  Sponsor: Ottawa Hospital Research Institute

PhaseNA
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

PANTHER-GI Pilot Study will assess the feasibility of a full-scale multicentre cohort management study evaluating the safety of a standardized strategy for resuming direct oral anticoagulants (DOACs) after major DOAC-related gastrointestinal (GI) bleeding among patients at moderate to high risk of re-bleeding and thrombosis. A parallel registry will assess whether eligible patients who are not enrolled in the PANTHER-GI Pilot Study are systematically different than enrolled patients and to explore barriers to enrolment.

This description comes directly from the study's public registry record.

Talk to the study team

Deborah M Siegal, MD  ·  613-737-8899  ·  dsiegal@toh.ca

Always discuss trial participation with your own doctor first.

Locations (2)

Alberta Health Services - Peter Lougheed Center Endoscopy UnitCalgary, Alberta, CanadaRecruiting
Ottawa Hospital Research InstituteOttawa, Ontario, CanadaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05290857