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Efficacy and Clinical Outcomes of Levosimendan in E-CPR (ECPR)

Hamad Medical Corporation (HMC) logo

Hamad Medical Corporation (HMC)

Status

Enrolling

Conditions

Extracorporeal Membrane Oxygenation Complication
Cardiogenic Shock

Treatments

Drug: Levosimendan

Study type

Observational

Funder types

Industry

Identifiers

NCT05730907
MRC-01-21-282

Details and patient eligibility

About

Treatment of refractory cardiac arrest requiring cardiopulmonary resuscitation (CPR) may be augmented with Extracorporeal membrane oxygenation (ECMO) to re-establish perfusion in the absence of return of spontaneous circulation. Literature has demonstrated that ECMO initiated during advanced cardiopulmonary life support may confer superior survival rates with acceptable survival and a relatively low incidence of significant neurologic impairment. Levosimendan has not been investigated in patients with cardiac arrest who underwent Extracorporeal CPR (E-CPR). The current study aims to examine whether levosimendan use in the aforementioned patient population could improve survival and ECMO parameters.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

IInclusion criteria:

  • Hospitalized patients ≥ 18 years of age at the time of E-CPR use
  • Patients suffered cardiac arrest (IHCA or OHCA)
  • Patients received VA-ECMO for E-CPR
  • Criteria as per HMC's Extracorporeal Membrane Oxygenation (ECMO) for Cardiac Arrest (E-CPR) clinical practice guidelines (attached with the study protocol)

Exclusion criteria:

  • Patients with incomplete key data
  • Criteria as per HMC's Extracorporeal Membrane Oxygenation (ECMO) for Cardiac Arrest (E-CPR) clinical practice guidelines (attached with the study protocol)

Trial contacts and locations

1

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Central trial contact

Rasha Kaddoura, Msc; Bssant Orabi, Msc

Data sourced from clinicaltrials.gov

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