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CAERvest® - A Novel Endothermic Hypothermic Device for Core Body Cooling. Safety and Efficacy Testing.

Primary Purpose

Hypothermia.

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Cooling
Sponsored by
Bodychillz Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypothermia. focused on measuring hypothermia, induced, rewarming, therapeutic, heart arrest, asystole, frostbite

Eligibility Criteria

18 Years - 35 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Human volunteers aged over 18. The upper age limit, as is standard for risk mitigation in such studies, is 35. The volunteer must have capacity to understand the trial and give informed consent to participate. If the volunteer's first language is not English we will make use of Sussex Interpreting Services, a professional interpreting service.

Exclusion Criteria:

Pregnancy. Any disclosed medical condition. Any medical condition detected on examination. Core temperature outside stated parameters.

We will ask the volunteer to confirm that they are otherwise healthy, taking no regular medication (except the oral contraceptive pill), are not using recreational drugs and have no significant past medical history, in particular cardiovascular disease of any sort, thyroid disease, diabetes mellitus or other metabolic disease.

Sites / Locations

  • CIRU, Royal Sussex County Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Cooling

Arm Description

Outcomes

Primary Outcome Measures

Reduction in core body temperature by 1 degree Centigrade.
The cooling properties of the vest are under investigation, and this reduction is the primary outcome measure.

Secondary Outcome Measures

Skin condition.
As the cooling is performed by a cold vest applied directly to the skin we need to ensure that no skin damage is caused.
ECG abnormalities.
ECG abnormalities: ECG abnormalities are common after cardiac arrest, and have been noted in cooled patients after cardiac arrest. We will monitor the ECG for any abnormalities. The following will be noted but will not terminate the study: Bradycardia of less than 15 beats per minute below baseline. Unifocal ventricular ectopics. Unifocal atrial ectopics. Any other cardiac abnormality will cause immediate termination of the study and intervention to treat as necessary. A defibrillator will be available in the study room.
Sepsis.
Sepsis: Increased rates of sepsis have been seen in intensive care units in patients who have received therapeutic hypothermia. We will enquire about sepsis symptoms in our follow-up contact.
Skin condition.
Our aim is not to cause any skin damage to patients or volunteers. We will therefore inspect the skin after removing the vest or at any time before that if the volunteer expresses concern. We expect pallor of the skin during cooling and reddening during rewarming with some numbness and some discomfort, both during cooling and rewarming. We will regard any evidence of frostbite as a serious untoward injury (SUI) and this will result in suspension of the study and an investigation into the specific vest used and the general vest design and formulation. We regard this as a serious risk but highly unlikely in practice.

Full Information

First Posted
January 7, 2014
Last Updated
March 3, 2014
Sponsor
Bodychillz Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT02030236
Brief Title
CAERvest® - A Novel Endothermic Hypothermic Device for Core Body Cooling. Safety and Efficacy Testing.
Official Title
CAERvest® - A Novel Endothermic Hypothermic Device for Core Body Cooling. Safety and Efficacy Testing.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Unknown status
Study Start Date
March 2014 (undefined)
Primary Completion Date
May 2014 (Anticipated)
Study Completion Date
May 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bodychillz Ltd

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Cooling the whole body to 32-34 degrees Centigrade from the normal of around 37 degrees Centigrade for 24 hours has been shown to be an effective way of reducing damage to brain function after return of spontaneous circulation when someone has been resuscitated from cardiac arrest. Cardiac arrest is a form of heart attack where the heart stops pumping. The device is a prototype cooling vest. The investigators anticipate that this will be useful in ambulances, helicopters and emergency departments where there is a need for a portable, safe, easy-to-use, inexpensive, external, effective, readily-controlled and single-patient use device able to reduce body temperature by at least 1 degree Centigrade an hour to initiate cooling. What the investigators are doing in these trials is to demonstrate that the investigators can cool people and to get the best design possible for patient use. That means some of the initial prototypes will not resemble what we expect the eventual device to look like. The investigators will be undertaking the initial trials on 30 normal volunteers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypothermia.
Keywords
hypothermia, induced, rewarming, therapeutic, heart arrest, asystole, frostbite

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cooling
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Cooling
Other Intervention Name(s)
CAERvest prototype
Intervention Description
Temperature reached Duration of exposure to cold.
Primary Outcome Measure Information:
Title
Reduction in core body temperature by 1 degree Centigrade.
Description
The cooling properties of the vest are under investigation, and this reduction is the primary outcome measure.
Time Frame
1 hour.
Secondary Outcome Measure Information:
Title
Skin condition.
Description
As the cooling is performed by a cold vest applied directly to the skin we need to ensure that no skin damage is caused.
Time Frame
3 days.
Title
ECG abnormalities.
Description
ECG abnormalities: ECG abnormalities are common after cardiac arrest, and have been noted in cooled patients after cardiac arrest. We will monitor the ECG for any abnormalities. The following will be noted but will not terminate the study: Bradycardia of less than 15 beats per minute below baseline. Unifocal ventricular ectopics. Unifocal atrial ectopics. Any other cardiac abnormality will cause immediate termination of the study and intervention to treat as necessary. A defibrillator will be available in the study room.
Time Frame
3 hours.
Title
Sepsis.
Description
Sepsis: Increased rates of sepsis have been seen in intensive care units in patients who have received therapeutic hypothermia. We will enquire about sepsis symptoms in our follow-up contact.
Time Frame
3 days.
Title
Skin condition.
Description
Our aim is not to cause any skin damage to patients or volunteers. We will therefore inspect the skin after removing the vest or at any time before that if the volunteer expresses concern. We expect pallor of the skin during cooling and reddening during rewarming with some numbness and some discomfort, both during cooling and rewarming. We will regard any evidence of frostbite as a serious untoward injury (SUI) and this will result in suspension of the study and an investigation into the specific vest used and the general vest design and formulation. We regard this as a serious risk but highly unlikely in practice.
Time Frame
3 days.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Human volunteers aged over 18. The upper age limit, as is standard for risk mitigation in such studies, is 35. The volunteer must have capacity to understand the trial and give informed consent to participate. If the volunteer's first language is not English we will make use of Sussex Interpreting Services, a professional interpreting service. Exclusion Criteria: Pregnancy. Any disclosed medical condition. Any medical condition detected on examination. Core temperature outside stated parameters. We will ask the volunteer to confirm that they are otherwise healthy, taking no regular medication (except the oral contraceptive pill), are not using recreational drugs and have no significant past medical history, in particular cardiovascular disease of any sort, thyroid disease, diabetes mellitus or other metabolic disease.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rowland L Cottingham, FRCS FCEM
Phone
+44 1273 696955
Email
rowley.cottingham@bodychillz.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rowland L Cottingham, FRCS FCEM
Organizational Affiliation
Brighton and Sussex Universities Hospital NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
CIRU, Royal Sussex County Hospital
City
Brighton
ZIP/Postal Code
BN2 5BE
Country
United Kingdom
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rowland L Cottingham, FRCS FCEM

12. IPD Sharing Statement

Citations:
PubMed Identifier
11856793
Citation
Hypothermia after Cardiac Arrest Study Group. Mild therapeutic hypothermia to improve the neurologic outcome after cardiac arrest. N Engl J Med. 2002 Feb 21;346(8):549-56. doi: 10.1056/NEJMoa012689. Erratum In: N Engl J Med 2002 May 30;346(22):1756.
Results Reference
background
PubMed Identifier
21435740
Citation
Seupaul RA, Wilbur LG. Evidence-based emergency medicine. Does therapeutic hypothermia benefit survivors of cardiac arrest? Ann Emerg Med. 2011 Sep;58(3):282-3. doi: 10.1016/j.annemergmed.2011.02.002. Epub 2011 Mar 24. No abstract available.
Results Reference
background
Links:
URL
http://www.bsms.ac.uk/research/ciru/
Description
Our study location.
URL
http://www.hra.nhs.uk/
Description
UK health regulatory authority.
URL
http://www.mhra.gov.uk/Aboutus/index.htm
Description
The UK MHRA.

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CAERvest® - A Novel Endothermic Hypothermic Device for Core Body Cooling. Safety and Efficacy Testing.

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