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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00827957
Other study ID # CIRB 2008/080/C
Secondary ID
Status Completed
Phase Phase 4
First received January 21, 2009
Last updated February 9, 2017
Start date October 2008
Est. completion date October 2014

Study information

Verified date February 2017
Source Singapore General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Controlled therapeutic hypothermia is a method of preserving neurological function post-resuscitation.It has been associated with improved functional recovery and reduced histological deficits in animal models of cardiac arrest.


Description:

Three randomized clinical studies have been reported showing improved neurological outcome and reduced mortality in post-resuscitation patients treated with hypothermia compared to controls. Of the various methods of inducing hypothermia, internal cooling using an endovascular catheter and external cooling using gel pads with a water based circulating system have shown the most promise. There have not been any studies looking at outcomes between the two methods of cooling.


Recruitment information / eligibility

Status Completed
Enrollment 51
Est. completion date October 2014
Est. primary completion date October 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

1. Sustained return of spontaneous circulation (ROSC) after cardiac arrest, for more than 30 min

2. Patients aged between 18 to 80 years.

3. Patients who are hemodynamically stable, with a systolic BP > 90 mmHg with or without inotropic support.

4. Patients comatose or unresponsive post-resuscitation

Exclusion Criteria:

1. Hypotension despite fluid and/or vasopressor support

2. Positive pregnancy test in women below 50 years

3. Premorbid status bedbound and uncommunicative

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Internal Cooling
The intravascular cooling system uses a single lumen (8.5 Fr,38 cm) central venous catheter inserted into the inferior vena cava via the left or right femoral vein. Normal saline is pumped through three balloons mounted on the catheter and returned to a central system in a closed loop. The saline flow within the balloons is in close contact with the patient's blood flow and serves as a heat exchange system. An automatic temperature control device adjusts the temperature of the circulating saline (4°C to 42°C) based on the patient's core temperature.
External Cooling
The gel-coated external cooling device consists of four water circulating gel coated energy transfer pads, and is placed on the patient's back, abdomen, and both thighs. Depending on the size used, the total surface area ranges between 0.60 and 0.77 m2. It is connected to an automatic thermostat controlling the temperature of the circulating water (4°C to 42°C) based on the patient's core temperature.

Locations

Country Name City State
Singapore National Heart Centre Singapore Singapore
Singapore Singapore General Hospital Singapore

Sponsors (2)

Lead Sponsor Collaborator
Singapore General Hospital National Heart Centre Singapore

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival to hospital discharge 30 days post arrest
Secondary Neurological status of post-resuscitation patients 1 year post discharge
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