Body Cooling During Carotid Endarterectomy: No-profit, Open, Mono-centric, Feasibility Study
Primary Purpose
Carotid Artery Diseases, Hypothermia, Stroke
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
endovascular cooling (Zoll system)
Sponsored by
About this trial
This is an interventional prevention trial for Carotid Artery Diseases focused on measuring carotid endarterectomy, stroke, hypothermia, endovascular cooling
Eligibility Criteria
Inclusion Criteria:
- Subject eligible for CEA, without progression of symptoms, with low (<4) Anesthesia Risk Assessment
- Age ≥ 18 years;
- Written informed consent
Exclusion Criteria:
- Evidence from a CT or MRI scan or from other pre-inclusion investigations of an intracranial haemorrhage, a tumour, encephalitis, or any diagnosis of acute brain focal lesion;
- Progression or instability of neurological status
- Conditions that may be exacerbated by hypothermia, such as haematological dyscrasias, oral anticoagulant treatment with INR ≥ 1.7, severe pulmonary disease, severe heart failure (defined as a New York Heart Association (NYHA) score of III or IV), history of myocardial infarction within the previous 3 months, angina pectoris in the previous 3 months, severe infection with a C-reactive protein > 50 mg/dl, or a clinical diagnosis of sepsis;
- Blood oxygen saturation below 94%, allowing a maximum of 2 L/min oxygen delivered nasally to achieve this;
- Bradycardia (<40 beats/min);
- Body weight > 120 kg;
- Severe hepatic dysfunction, or severe renal dysfunction;
- Pregnancy. Women of childbearing potential are excluded unless a negative test for pregnancy has been obtained prior to randomisation;
- Other serious illness that may confound treatment assessment or increase the risks of cooling;
- Social or other conditions that according to the investigator's judgement might be a major problem for follow-up.
Sites / Locations
- NESMOS Department St. Andrea Hospital
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Single arm
Arm Description
The endovascular cooling system will be Zoll IVTM. This system consists of a control module (either CoolGard 3000 or Thermogard XP), a CoolGard start-up kit, and an ICY catheter (either IC-3585 AE or IC-3585)
Outcomes
Primary Outcome Measures
Adverse events
Severe adverse events were defined as any life-threatening event including pneumonia (diagnosed on the basis of clinical signs or symptoms), myocardial infarction and parenchymal hemorrhage. Non-severe safety outcomes included incidence of bradycardia (<40 beats per minute), cardiac arrhythmia, hypertension, hypotension and any coagulation disorders.
Secondary Outcome Measures
Full Information
NCT ID
NCT02629653
First Posted
December 10, 2015
Last Updated
December 11, 2015
Sponsor
S. Andrea Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02629653
Brief Title
Body Cooling During Carotid Endarterectomy: No-profit, Open, Mono-centric, Feasibility Study
Official Title
Body Cooling During Carotid Endarterectomy: No-profit, Open, Mono-centric, Feasibility Study
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
December 2013 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
December 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
S. Andrea Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Aim of the study is to determine whether endovascular systemic cooling to a target temperature of 34-35°C initiated before, and maintained during Carotid EndoArterectomy (CEA), is feasible and safe
Detailed Description
The study is based on the hypothesis that performing CEA during hypothermia substantially reduces the risk due to a potential, temporary hypoperfusion, associated with the surgical procedure.
The rationale behind the study is based on the assumption that Carotid EndArterectomy (CEA), by removing local causes of downstream altered circulation, improves cerebral hemodynamics and provides an effective prevention of stroke and TIA. The intervention itself, however, causes immediate risk of stroke or death, and it is also an issue whether the temporary reduction of blood flow associated with clamping of the artery, during the surgical intervention, may trigger long-lasting brain tissue dysfunction.
Mild hypothermia (34-35 °C) is probably the most effective approach to protect the brain from ischemic insults. Most of the supportive data were obtained in animal models of ischemia. Several phase II trials have shown safety and feasibility of cooling subjects with stroke, in the hours following onset of symptoms. Early interventions show the highest benefit.
Eligible patients will initiate cooling 60-90 min before CEA with endovascular cooling (Zoll system) to the target 34-35°C (assessed by bladder thermometer). The Zoll IVTM system is an endovascular cooling system that consists of a control module (either CoolGard 3000 or Thermogard XP), a CoolGard start-up kit, an ICY catheter (either IC-3585 AE or IC-3585 CO or IC-3893 AE or IC-3893 CO), a catheter convenience kit for catheter insertion (CO models only), thermal probes and cables. All the devise component have CE mark. The Low temperature will be maintained during the CEA procedure, followed by gradual, passive, controlled rewarming (0.4 °C/h). Type of anaesthesia will be decided according to good clinical practice. The cooling procedure will be, therefore, carried out during the anaesthesia procedure required by the surgical intervention. There is a chance that the duration of the anaesthesia will be longer that required, but all the efforts will be undertaken to keep the anaesthesia time as short as if there were no cooling
Clinical and instrumental evaluations will be carried out before and post intervention. Each evaluation will consist of physical examination, neuropsychological evaluation (MoCA test), blood tests and brain MRI or TC.
Safety is evaluated on the basis of severe adverse event
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carotid Artery Diseases, Hypothermia, Stroke, Carotid Artery Plaque, Carotid Artery Stenosis, Cerebrovascular Accident
Keywords
carotid endarterectomy, stroke, hypothermia, endovascular cooling
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single arm
Arm Type
Other
Arm Description
The endovascular cooling system will be Zoll IVTM. This system consists of a control module (either CoolGard 3000 or Thermogard XP), a CoolGard start-up kit, and an ICY catheter (either IC-3585 AE or IC-3585)
Intervention Type
Device
Intervention Name(s)
endovascular cooling (Zoll system)
Intervention Description
The Zoll IVTM is an endovascular cooling system that consists of a control module (either CoolGard 3000 or Thermogard XP), a CoolGard start-up kit, and an ICY catheter (either IC-3585 AE or IC-3585).
Primary Outcome Measure Information:
Title
Adverse events
Description
Severe adverse events were defined as any life-threatening event including pneumonia (diagnosed on the basis of clinical signs or symptoms), myocardial infarction and parenchymal hemorrhage. Non-severe safety outcomes included incidence of bradycardia (<40 beats per minute), cardiac arrhythmia, hypertension, hypotension and any coagulation disorders.
Time Frame
Any adverse event at 1 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subject eligible for CEA, without progression of symptoms, with low (<4) Anesthesia Risk Assessment
Age ≥ 18 years;
Written informed consent
Exclusion Criteria:
Evidence from a CT or MRI scan or from other pre-inclusion investigations of an intracranial haemorrhage, a tumour, encephalitis, or any diagnosis of acute brain focal lesion;
Progression or instability of neurological status
Conditions that may be exacerbated by hypothermia, such as haematological dyscrasias, oral anticoagulant treatment with INR ≥ 1.7, severe pulmonary disease, severe heart failure (defined as a New York Heart Association (NYHA) score of III or IV), history of myocardial infarction within the previous 3 months, angina pectoris in the previous 3 months, severe infection with a C-reactive protein > 50 mg/dl, or a clinical diagnosis of sepsis;
Blood oxygen saturation below 94%, allowing a maximum of 2 L/min oxygen delivered nasally to achieve this;
Bradycardia (<40 beats/min);
Body weight > 120 kg;
Severe hepatic dysfunction, or severe renal dysfunction;
Pregnancy. Women of childbearing potential are excluded unless a negative test for pregnancy has been obtained prior to randomisation;
Other serious illness that may confound treatment assessment or increase the risks of cooling;
Social or other conditions that according to the investigator's judgement might be a major problem for follow-up.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francesco Orzi, Prof, MD
Organizational Affiliation
NESMOS Department, University of Rome "La Sapienza"; St. Andrea Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
NESMOS Department St. Andrea Hospital
City
Rome
ZIP/Postal Code
00189
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
24047063
Citation
Grotta JC. Clinical practice. Carotid stenosis. N Engl J Med. 2013 Sep 19;369(12):1143-50. doi: 10.1056/NEJMcp1214999. No abstract available.
Results Reference
result
PubMed Identifier
24761406
Citation
Lee JH, Suh BY. Risk factor analysis of new brain lesions associated with carotid endarterectmy. Ann Surg Treat Res. 2014 Jan;86(1):39-44. doi: 10.4174/astr.2014.86.1.39. Epub 2014 Jan 1.
Results Reference
result
PubMed Identifier
7723155
Citation
Endarterectomy for asymptomatic carotid artery stenosis. Executive Committee for the Asymptomatic Carotid Atherosclerosis Study. JAMA. 1995 May 10;273(18):1421-8.
Results Reference
result
PubMed Identifier
22353781
Citation
Yenari MA, Han HS. Neuroprotective mechanisms of hypothermia in brain ischaemia. Nat Rev Neurosci. 2012 Feb 22;13(4):267-78. doi: 10.1038/nrn3174.
Results Reference
result
PubMed Identifier
12771566
Citation
Erecinska M, Thoresen M, Silver IA. Effects of hypothermia on energy metabolism in Mammalian central nervous system. J Cereb Blood Flow Metab. 2003 May;23(5):513-30. doi: 10.1097/01.WCB.0000066287.21705.21.
Results Reference
result
PubMed Identifier
23415567
Citation
Wu TC, Grotta JC. Hypothermia for acute ischaemic stroke. Lancet Neurol. 2013 Mar;12(3):275-84. doi: 10.1016/S1474-4422(13)70013-9.
Results Reference
result
PubMed Identifier
20354545
Citation
van der Worp HB, Macleod MR, Kollmar R; European Stroke Research Network for Hypothermia (EuroHYP). Therapeutic hypothermia for acute ischemic stroke: ready to start large randomized trials? J Cereb Blood Flow Metab. 2010 Jun;30(6):1079-93. doi: 10.1038/jcbfm.2010.44. Epub 2010 Mar 31.
Results Reference
result
PubMed Identifier
8542058
Citation
Kamme F, Campbell K, Wieloch T. Biphasic expression of the fos and jun families of transcription factors following transient forebrain ischaemia in the rat. Effect of hypothermia. Eur J Neurosci. 1995 Oct 1;7(10):2007-16. doi: 10.1111/j.1460-9568.1995.tb00623.x.
Results Reference
result
PubMed Identifier
27058874
Citation
Candela S, Dito R, Casolla B, Silvestri E, Sette G, Filippi F, Taurino M, Brancadoro D, Orzi F. Hypothermia during Carotid Endarterectomy: A Safety Study. PLoS One. 2016 Apr 8;11(4):e0152658. doi: 10.1371/journal.pone.0152658. eCollection 2016.
Results Reference
derived
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Body Cooling During Carotid Endarterectomy: No-profit, Open, Mono-centric, Feasibility Study
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