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Cognitive Dysfunction after Anesthesia (CoDA) Study

Cognitive Dysfunction after Anesthesia (CoDA) Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-09000704
Enrollment
Unknown
Registered
2007-09-12
Start date
2005-01-01
Completion date
Unknown
Last updated
2019-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

Interventions

Two groups:Neurophysiology guided Anaesthesia Intraoperative period versus Routine care

Sponsors

RGC
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1) Patients aged >= 60 years with an American Society of Anesthesiologists physical status of between 1 and 4 who have been scheduled for elective non-cardiac surgery; (2) Surgery expected to last for 2 hours or longer with an anticipated hospital stay of at least 4 days.

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) Patients not expected to be available for, or cooperate with, perioperative interviews; (2) Patients with major psychosis who are taking tranquillizers or antidepressants; (3) Patients with disease of the central nervous system, including known or suspected dementia or memory impairment (defined as a Mini-Mental State Examination score of <=23); (4) Patients with illiteracy, significant hearing or visual impairment, or language difficulties will also be excluded.

Design outcomes

Primary

MeasureTime frame
Cognitive function using neuropsychologic tests;

Secondary

MeasureTime frame
(1) Recovery time (2) Quality of recovery (3) Major perioperative complications;

Countries

China

Contacts

Public ContactMatthew Chan

Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong

mtvchan@cuhk.edu.hk+852 26322736

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026