Coronary Artery Disease Clinical Trial
Official title:
Noninvasive Neuromonitoring of Surgery of the Thoracic Aorta
Verified date | August 2016 |
Source | Helsinki University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Finland: Ethics Committee |
Study type | Observational |
The aim of this prospective, explorative study of noninvasive neuromonitoring was to search potential and practical methods associated with neurological outcome in the perioperative and immediate postoperative setting of surgery of the thoracic aorta. These methods include abbreviated EEG monitoring, near-infrared spectroscopy, transcranial Doppler ultrasound and biochemical markers associated with neuronal damage.
Status | Completed |
Enrollment | 61 |
Est. completion date | November 2011 |
Est. primary completion date | November 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients scheduled for elective or emergency surgery on the thoracic aorta (study group) or coronary heart disease (control groups) - Informed consent from patient or next of kin Exclusion Criteria: - Age under 18 years |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Finland | Helsinki University Central Hospital, Department of Cardiac Surgery | Helsinki | Uudenmaan lääni |
Lead Sponsor | Collaborator |
---|---|
Helsinki University | GE Healthcare |
Finland,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Neurological outcome | Permanent neurological damage or death within monitoring period (up to 48 h after surgery) | Monitoring period from anesthesia induction to 48 hours after end of surgery | No |
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