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NCT04216394

Anticoagulation in Emergency General Surgery

Completed Last updated 27 March 2026
What this trial tests

trial testing Emergency general surgery in Emergency General Surgery in 4 participants. Completed in 13 November 2020.

Timeline
31 October 2019
Primary endpoint
13 November 2020
13 November 2020

Quick facts

Lead sponsorMethodist Health System
StatusCompleted
Study typeOBSERVATIONAL
Enrollment4
Start date31 October 2019
Primary completion13 November 2020
Estimated completion13 November 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Methodist Health System — full company profile →

Who can join

18 and older, any sex, with Emergency General Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

While DOACs are increasing in use in the EGS patient population, the risk of bleeding and the reversal of these agents to reduce hemorrhage is still evolving. Given the paucity of data regarding the impact of DOACs in this patient population, it becomes empiric to identify bleeding patterns and outcomes in the EGS population taking DOACs. We hypothesize that patients taking a DOAC will have a higher bleeding incidence and need for an unplanned intervention secondary to hemorrhage in EGS patients undergoing an urgent or emergent operation when compared to patients taking warfarin and antiplatelets.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Methodist Health System trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04216394.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing