Prospective Observational Study of Perioperative Stroke: A Pilot Study

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-ONC-12002073

Enrollment

Unknown

Registered

2012-04-04

Start date

2012-03-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Perioperative Stroke

Interventions

1:Anesthesia/Surgery

Duration of intervention:During Surgery

Eligibility

Sex/Gender

Male

Age

60 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Patients scheduled for noncardiac, non-neurological surgery receiving general and/or regional anesthetic; (2) Requiring at least 3 nights of hospital stay.

Exclusion criteria

Exclusion criteria: (1) Patients receiving only simple infiltrative (i.e. local) or topical anesthesia; (2) Patients previously enrolled in the study and patients who do not consent to participate will also be excluded

Design outcomes

Primary

Measure	Time frame
Stroke within 30 days after surgery;	—

Secondary

Measure	Time frame
Perioperative major cardiovascular complications (including myocardial infarction, pulmonary embolism, arrhythmias, congestive heart failure, cardiac death);	—

Countries

China

Contacts

Public ContactMatthew Chan

mtvchan@cuhk.edu.hk+852 2632 2736

Outcome results

None listed

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