NCT05306821RecruitingNot Applicable
Effectiveness of Interventions for Hospital Medical Thromboprophylaxis: a Bicentric Swiss Quality-improvement Study
Marc Blondon2 sites in 1 country600 target enrollmentStarted: September 1, 2020Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 600
- Locations
- 2
- Primary Endpoint
- Proportion of patients with an adequate thromboprophylaxis
Study Overview
Brief Summary
The primary objective is to evaluate and compare the short-term and medicum-term effectiveness of 2 types of interventions in 2 different hospitals to improve the adequacy of hospital thromboprophylaxis among acute medical inpatients.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •acute medical inpatients hospitalized at the Geneva University Hospitals or the Lugano Regional Hospitals
Exclusion Criteria
- •patients already on therapeutic anticoagulation
- •patients with an estimated life expectancy of <3 months
- •pregnancy
- •patients hospitalized for COVID-19
Arms & Interventions
Implementation of an electronic tool for risk stratification and thromboprophylaxis prescription
Experimental
Intervention: Educative sessions (Other)
Implementation of educative sessions and pocket cards for thromboprophylaxis
Experimental
Intervention: Pocket card (Other)
Implementation of educative sessions and pocket cards for thromboprophylaxis
Experimental
Intervention: Educative sessions (Other)
Implementation of an electronic tool for risk stratification and thromboprophylaxis prescription
Experimental
Intervention: Comprehensive electronic tool in the electronic medical chart (Other)
Outcomes
Primary Outcomes
Proportion of patients with an adequate thromboprophylaxis
Time Frame: 90 days
Secondary Outcomes
- Incidence of major bleeding(90 days)
- Incidence of venous thromboembolism(90 days)
Investigators
Marc Blondon
Principal Investigator
University Hospital, Geneva
Study Sites (2)
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