A cohort study of the perioperative patients

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000034039

Enrollment

Unknown

Registered

2020-06-21

Start date

2020-09-01

Completion date

Unknown

Last updated

2020-06-22

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

Conditions

Stress-related disorders

Interventions

Case series:Nil

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with aged >=18 years old; 2. Patients who plan to undergo selective surgery; 3. Permanent residents of Sichuan Province (unlimited household registration).

Exclusion criteria

Exclusion criteria: 1. Patients with local anesthesia; 2. Patients undergoing cardiac surgery; 3. Patients undergoing daytime surgery.

Design outcomes

Primary

Measure	Time frame
perioperative complication;	—

Secondary

Measure	Time frame
all-cause mortality after surgery;NRS scores at different time points after surgery;Incidence of PTSD after surgery;length of stay;Hospitalization Expense;	—

Contacts

Public ContactHuan Song

Department of Anesthesiology and Critical Care Medicine, West China Hospital, Sichuan University

songhuan@wchscu.cn+86 19983137876

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026