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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02827422
Other study ID # 2015-P33001-00
Secondary ID
Status Recruiting
Phase N/A
First received July 5, 2016
Last updated October 19, 2016
Start date October 2015
Est. completion date June 2019

Study information

Verified date October 2016
Source Seoul St. Mary's Hospital
Contact Kyu Nam Park, MD, PhD
Phone 82-2-2258-6301
Email emsky@catholic.ac.kr
Is FDA regulated No
Health authority Korea: Ministry for Health and Welfare
Study type Observational [Patient Registry]

Clinical Trial Summary

Therapeutic hypothermia after out-of-hospital cardiac arrest is considered as a standard care. However, optimal candidates, optimal dose, duration, timing of initiation and rate of rewarming is still unknown. The objective of this project is to improve the outcomes for patients after resuscitation from out-of-hospital cardiac arrest treated with therapeutic hypothermia established from the analysis of multicenter registry data.


Recruitment information / eligibility

Status Recruiting
Enrollment 1800
Est. completion date June 2019
Est. primary completion date June 2019
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age of older than 18 years

- out-of-hospital cardiac arrest

- comatose mentality after return of spontaneous circulation (ROSC)

- treated with therapeutic hypothermia, regardless of target temperature

Exclusion Criteria:

- suspected or confirmed to cerebrovascular accident

- poor pre-arrest neurologic status (CPC>3)

- patients who are terminally ill or for whom intensive care dose not seem to be appropriate

- Do not attempt resuscitation (DNAR) order

- patients with tympanic membrane temperature below 30 degree celsius on admission

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
not provided


Locations

Country Name City State
Korea, Republic of Seoul St. Mary's Hospital, The Catholic University of Korea Seoul

Sponsors (1)

Lead Sponsor Collaborator
Kyu Nam Park

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary survival 6 months after cardiac arrest Yes
Primary Neurologic Outcome Cerebral Performance Category (CPC). CPC 1,2 : Good Outcome CPC 3,4,5 : Poor Outcome 6 months after cardiac arrest Yes
Primary Neurologic Outcome modified Rankin Scale (mRS) mRS 0,1,2, 3 : Good Outcome mRS 4,5,6 : Poor Outcome after 6 months Yes
Secondary survival duration of hospitalization, limit 180 days Yes
Secondary neurological outcome Cerebral Performance Category (CPC). CPC 1,2 : Good Outcome CPC 3,4,5 : Poor Outcome duration of hospitalization, limit 180 days Yes
Secondary neurological outcome modified Rankin Scale (mRS) mRS 0,1,2, 3 : Good Outcome mRS 4,5,6 : Poor Outcome duration of hospitalization, limit 180 days Yes
Secondary Survival 1 month after cardiac arrest Yes
Secondary neurological outcome Cerebral Performance Category (CPC). CPC 1,2 : Good Outcome CPC 3,4,5 : Poor Outcome 1 month after cardiac arrest Yes
Secondary neurological outcome modified Rankin Scale (mRS) mRS 0,1,2, 3 : Good Outcome mRS 4,5,6 : Poor Outcome 1 month after cardiac arrest Yes
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