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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00329563
Other study ID # 25186
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received May 22, 2006
Last updated April 13, 2017
Start date November 2004
Est. completion date March 2006

Study information

Verified date April 2017
Source University of Washington
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall goal of this study is to determine the feasibility of initiating hypothermia in cardiac arrest patients as soon as possible in the field. In this pilot study we will randomize 125 patients after return of spontaneous circulation (ROSC) to hypothermia with rapid infusion of 2 liters of 4oC Normal Saline IV solution over 20 to 30 minutes, IV sedation and muscle paralysis or to standard of care following ROSC. The primary objectives of this study will be to determine whether temperature of 33-34oC can be achieved and maintained using this strategy. The primary outcome measures will include: temperature changes of the patients at time of admission to the hospital. Secondary analysis will include determining if the proportion of patients discharged from the hospital is increased in the group receiving hypothermia. If this initial pilot study can demonstrate feasibility in achieving and maintaining hypothermia, a larger randomized clinical trial to test the hypothesis that hypothermia initiation in the field will increase the proportion of patients surviving following cardiac arrest will be planned.


Recruitment information / eligibility

Status Completed
Enrollment 125
Est. completion date March 2006
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Resuscitated out-of-hospital cardiac arrest defined as having a palpable pulse comatose IV access Intubated

Exclusion Criteria:

- age less than 18 traumatic cause of cardiac arrest

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Up to 2 liter infusion of cold 4 degree C normal saline
Patients randomized to field cooling will receive up to 2 liters of 4oC normal saline. Control patients will receive standard of care following resuscitation.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Washington Medic One Foundation

Outcome

Type Measure Description Time frame Safety issue
Primary Temperature difference between first field temperature and hospital arrival temperature less than 60 minutes
Secondary Survival to discharge from hospital Between 2 -30 days
Secondary Awakening in the hospital between 2-30 days
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