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EKOS in Patients With Pulmonary Embolism (PE)

Completed
Conditions
Pulmonary Embolism
Interventions
Drug: ECOS
Drug: Control group
Registration Number
NCT06738108
Lead Sponsor
Beni-Suef University
Brief Summary

A retrospective cohort study assessed patients who underwent EKOS intervention following the failure of initial therapeutic anticoagulation for managing acute pulmonary embolism at a tertiary hospital.

Detailed Description

A retrospective cohort study assessed patients who underwent EKOS intervention following the failure of initial therapeutic anticoagulation for managing acute pulmonary embolism at a tertiary hospital. Patients aged at least 18 years with a diagnosis of submassive or massive acute PE were included. Patients were excluded if they either did not receive EKOS intervention or were presented with stable PE. The primary outcome was the change in RV/LV diameter ratio from baseline to first outpatient follow-up.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
104
Inclusion Criteria
  • Patients ≥ 18 years diagnosed with massive or submassive acute PE.
Exclusion Criteria
  1. Patients presented with stable PE
  2. Patients did not receive EKOS intervention.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
ECOS groupECOSECOS
Control groupControl groupIV infusion tpa
Primary Outcome Measures
NameTimeMethod
The change in RV/LV diameter ratioone month

The change in RV/LV diameter ratio from baseline to first outpatient follow-up as documented on an echocardiogram.

Secondary Outcome Measures
NameTimeMethod
All-cause 30-day readmissionone month

All-cause 30-day readmission

Trial Locations

Locations (1)

Saudi German Hospital

🇪🇬

Cairo, Egypt

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