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NCT05306821 Clinical Trial

Effectiveness of Interventions for Hospital Medical Thromboprophylaxis: a Bicentric Swiss Quality-improvement Study

Venous Thromboembolism Clinical Trial

— TPX-ENHANCE  

Official title:
Effectiveness of Interventions for Hospital Medical Thromboprophylaxis: a Bicentric Swiss Quality-improvement Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05306821
Other study ID # 2019-01976
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 1, 2020
Est. completion date December 31, 2024

Study information
Verified date May 2023
Source University Hospital, Geneva
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Recruiting
Enrollment 600
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Comprehensive electronic tool in the electronic medical chart
Use of a comprehensive electronic tool in the electronic medical chart to help the stratification of risk of VTE and the subsequent prescription of an adequate thromboprophylaxis
• Educative sessions
Educative sessions on thromboprophylaxis
• Pocket card
Pocket card (guide for thromboprophylaxis)

Locations
Country Name City State
Switzerland Geneva University Hospitals Geneva
Switzerland Ospedale Regionale di Lugano Lugano

Sponsors (1)
Lead Sponsor Collaborator
Marc Blondon

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Proportion of patients with an adequate thromboprophylaxis 90 days
Secondary Incidence of venous thromboembolism 90 days
Secondary Incidence of major bleeding 90 days
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