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EKOS in Patients With Pulmonary Embolism (PE)

B

Beni-Suef University

Status

Completed

Conditions

Pulmonary Embolism

Treatments

Drug: Control group
Drug: ECOS

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full 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.

Enrollment

104 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

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.

Trial design

104 participants in 2 patient groups

ECOS group
Description:
ECOS
Treatment:
Drug: ECOS
Control group
Description:
IV infusion tpa
Treatment:
Drug: Control group

Trial contacts and locations

1

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Central trial contact

Asmaa A Elsayed

Data sourced from clinicaltrials.gov

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