Skip to content

Repository for Sepsis and Postresuscitation Samples

Repository for Samples Collected From Sepsis and Postresuscitation Patients in Emergency Intensive Care Unit

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01670383
Enrollment
500
Registered
2012-08-22
Start date
2006-07-31
Completion date
2028-12-31
Last updated
2023-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest, Sepsis

Keywords

Cardiac Arrest, Sepsis, Biological Markers, Anti-Inflammation Agents, Antioxidants

Brief summary

The objective of this study is to find a new therapeutic strategy by investigating the serial serum samples of patients with sepsis or postresuscitation state.

Interventions

None listed

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age over 16 years old * Admitted to ICU * Diagnosed as having sepsis or as postresuscitation status * Definition of sepsis: 2 or more SIRS criteria + infection is suspected * Definition of postresuscitation status: Survived from non-traumatic cardiac arrest

Exclusion criteria

* refusal to participate * DNAR status

Design outcomes

Primary

MeasureTime frameDescription
1-month mortality1 monthAll cause mortality within 1-month

Secondary

MeasureTime frameDescription
Hospital mortalityuntil hospital discharge, an expected average of 2 weeksAll cause mortality during hospitalization
ICU length of stayUntil ward transfer or discharge, an expected average of 7 days
Favorable neurologic outcomeat discharge, an expected average of 2 weeks and at 6-monthFavorable neurologic outcome is used for outcome measure in postresuscitation patients only. Favorable neurologic outcome means cerebral performance category 1 and 2. This outcome is measured at discharge and 6-month after admission.

Countries

South Korea

Contacts

Primary ContactKyung Su Kim, MD, PhD
kanesu@gmail.com82-10-8033-1127

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026