Status:
UNKNOWN
The Influence of Cognitive Decline on Quality of Life After Coronary Bypass
Lead Sponsor:
University Medical Center Groningen
Conditions:
Coronary Artery Bypass
Cognitive Dysfunction
Eligibility:
All Genders
18+ years
Brief Summary
During the last decades improvements in operative techniques and perioperative care have led to a steady decline in mortality after cardiac surgery. Good survival rates have been shown repeatedly alth...
Detailed Description
Study design: The investigators will conduct a prospective observational cohort study to evaluate QoL, cognitive decline and sarcopenia in adult patients after coronary artery bypass grafting. The in...
Eligibility Criteria
Inclusion
- adult patients scheduled for elective, isolated on-pump CABG
- able to stand and walk independently
- able to participate in the online screenings module for cognitive function to reduce the amount of missing data for cognitive function
Exclusion
- Pre-existing neurological deficits
- Psychiatric illness
- previous cardiac surgery
- pre-existing muscular diseases or missing extremities
- presence of an Internal Cardioverter Defibrillator (ICD), assist device or pacemaker
- large amounts of metal in or around the body
- inability to read or understand Dutch instructions
Key Trial Info
Start Date :
October 10 2018
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 31 2020
Estimated Enrollment :
140 Patients enrolled
Trial Details
Trial ID
NCT03774342
Start Date
October 10 2018
End Date
January 31 2020
Last Update
January 11 2019
Active Locations (1)
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1
University Medical Center Groningen
Groningen, Netherlands, 9700 RB