EKOS in Patients With Pulmonary Embolism (PE)
- Conditions
- Pulmonary Embolism
- Interventions
- Drug: ECOSDrug: 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
- Patients ≥ 18 years diagnosed with massive or submassive acute PE.
- Patients presented with stable PE
- Patients did not receive EKOS intervention.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description ECOS group ECOS ECOS Control group Control group IV infusion tpa
- Primary Outcome Measures
Name Time Method The change in RV/LV diameter ratio one month The change in RV/LV diameter ratio from baseline to first outpatient follow-up as documented on an echocardiogram.
- Secondary Outcome Measures
Name Time Method All-cause 30-day readmission one month All-cause 30-day readmission
Related Research Topics
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Trial Locations
- Locations (1)
Saudi German Hospital
🇪🇬Cairo, Egypt