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Clinical Trials/NCT03615300
NCT03615300
Terminated
Not Applicable

Predicting Long-term Outcomes After Cardiac Arrest by Using Serum NGAL: A Prospective, Observational Study

Uijeongbu St. Mary Hospital1 site in 1 country73 target enrollmentJune 28, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Out-of-Hospital Cardiac Arrest
Sponsor
Uijeongbu St. Mary Hospital
Enrollment
73
Locations
1
Primary Endpoint
Long term neurologic outcome
Status
Terminated
Last Updated
last year

Overview

Brief Summary

This study was performed to determine the prognosis of patients after cardiac arrest using serum markers called NGAL. The initial NGAL values of patients with post-cardiac arrest syndrome are checked by blood tests, and the long-term neurological prognosis and survival rate are collected after 6 months.

Detailed Description

Serum NGAL is currently being used as a test to determine the likelihood of developing renal failure. However, in a previous study, serum NGAL correlated with neurological prognosis in post cardiac arrest syndrome patients. This prospective study attempts to see the role of serum NGAL as a prognostic factor by including a sufficient number of patients.

Registry
clinicaltrials.gov
Start Date
June 28, 2018
End Date
May 1, 2022
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Uijeongbu St. Mary Hospital
Responsible Party
Principal Investigator
Principal Investigator

Joo Suk Oh, MD. PhD.

Professor

Uijeongbu St. Mary Hospital

Eligibility Criteria

Inclusion Criteria

  • Adult patients who underwent targeted temperature management after out-of-hospital cardiac arrest.

Exclusion Criteria

  • Patients who did not survived 3 days after cardiac arrest.
  • Pre-existing end-stage renal disease or dependence on renal replacement therapy

Outcomes

Primary Outcomes

Long term neurologic outcome

Time Frame: 6 months

Patients' CPC score after 6 months (good outcome : CPC score 1, 2 / poor outcome : CPC score 3, 4, 5)

Secondary Outcomes

  • Proportion of participants with Overall Survival at 6 months(6 months)

Study Sites (1)

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