Construction of a perioperative brain function monitoring and assessment system for high-risk coronary artery bypass graft patients

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300072149

Enrollment

Unknown

Registered

2023-06-05

Start date

2023-06-05

Completion date

Unknown

Last updated

2023-06-12

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

Conditions

Perioperative Nervous System Disorders

Interventions

Trail group:None

Eligibility

Sex/Gender

All

Age

18 Years to 120 Years

Inclusion criteria

Inclusion criteria: (1) Age = 18 years; (2) History of stroke or transient ischemic attack; (3) Presence of vascular risk factors, including intermittent claudication, internal carotid artery or intracranial artery stenosis >50%, history of endovascular stenting.

Exclusion criteria

Exclusion criteria: (1) Unwillingness to sign informed consent; (2) Unwillingness to accept follow-up visits.

Design outcomes

Primary

Measure	Time frame
Integrated brain and neck ultrasound;	—

Secondary

Measure	Time frame
Cognitive Performance;Emotion;Sleep;Neurophysiology;Neuroimaging;	—

Countries

China

Contacts

Public ContactShujuan Li

Fuwai Hospital Chinese Academy of Medical Sciences

lishujuan@fuwai.com+86 136 6120 7745

Outcome results

None listed

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