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Analysis of Endotoxin Activity in Patients With ECMO

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National Taiwan University

Status

Completed

Conditions

Cardiovascular Shock
Respiratory Failure

Treatments

Device: Extra-corporeal membrane oxygenation

Study type

Observational

Funder types

Other

Identifiers

NCT03978728
201811061RINC

Details and patient eligibility

About

Extra-corporeal membrane oxygenation (ECMO) can temporarily help patients gain time to wait for cardiopulmonary recovery or further treatment in patients with cardiopulmonary failure. Whether the blood flow provided by the ECMO can maintain the perfusion of various organs is an important factor affecting survival. Some ECMO patients died after the complication of sepsis. Our previous pilot analysis has recognized several ECMO patients with complicated sepsis has high endotoxin activity level. Endotoxemia can also occur in heart surgery and after cardiopulmonary bypass, trauma, organ transplantation, and out-of-hospital cardiac arrest patients. These trials used endotoxin activity analysis (EAA, EAATM, Spectral Diagnostics Inc., Canada) to analyze endotoxin activity. In addition, studies have indicated that the combination of procalcitonin (PCT) concentration and EAA activity can improve the accuracy of predicting sepsis. The primary aim of this study is to detect endotoxin activity in patients with ECMO support and compare whether the prognosis was associated with different level of EAA activity. The secondary aims are to analyze the risk factors leading to high EAA activity and investigate the diagnostic value of septic shock combining PCT examination. We suggest that the results of this study may help the ECMO medical team identify patients at high risk for septic shock and conduct adequate managements to improve patient survival and quality of life after survival.

Enrollment

55 patients

Sex

All

Ages

20 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with ECMO support

Exclusion criteria

  • < 20 years old or > 90 years old
  • not be able to collect blood sample within 48 hours after placement of ECMO
  • change plan to palliative care and plan to remove ECMO
  • non-native speakers

Trial design

55 participants in 1 patient group

ECMO patients
Description:
Patients with ECMO support
Treatment:
Device: Extra-corporeal membrane oxygenation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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