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Clinical Trials/ISRCTN68065962
ISRCTN68065962
Completed
未知

Investigation of neural mechanisms of COgnitive DEcline after Cardiac surgery with resting state fMRI (CODEC): a pilot study

niversity Hospitals Bristol NHS Foundation Trust0 sites20 target enrollmentAugust 8, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity Hospitals Bristol NHS Foundation Trust
Enrollment
20
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 8, 2018
End Date
February 9, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
niversity Hospitals Bristol NHS Foundation Trust

Eligibility Criteria

Inclusion Criteria

  • 1\. Aged between 60\-75 years
  • 2\. Electively referred for isolated coronary artery bypass grafting

Exclusion Criteria

  • 1\. Prisoners and adults lacking capacity to consent
  • 2\. Contraindications to MR (implanted electronic devices, metallic foreign bodies, claustrophobia, body weight \>140 kg or waist perimeter exceeding manufacturer's recommendations and others according to manufacturer’s recommendations and generally accepted guidelines)
  • 3\. Patients with a neurological disorder (e.g. epilepsy, Alzheimer’s, dementia and Parkinson’s disease)
  • 4\. Patients with a diagnosed psychiatric disorder (e.g. schizophrenia, psychosis), drug or alcohol addiction
  • 5\. Patients with an already identified as having cognitive impairment (e.g. memory and/or attentional deficits) as defined by psychometric assessment or a preoperative Mini\-mental State Examination score \< 24\. The Mini\-mental State Examination will be adminstered after consent but prior to any of the cognitive assessements or fMRI scan
  • 6\. Patients who have previously sustained a stroke, intra\-cerebral haemorrhage, acquired brain injury
  • 7\. Patients unable to complete the cognitive assessments required for the trial e.g. due to language difficulties, visual or hearing impairment

Outcomes

Primary Outcomes

Not specified

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