Establishment of a Risk Prediction Model for Postoperative Sleep Disturbance

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200066564

Enrollment

Unknown

Registered

2022-12-09

Start date

2022-12-01

Completion date

Unknown

Last updated

2024-05-13

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

Conditions

Postoperative sleep disturbances

Interventions

case series:none

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective surgery in our hospital; 2. Aged >=18 years; 3. ASA (American Society of Anesthesiologists Grading Standards) Grade I to III; 4. Patients were aware of the study protocol and agreed to participate.

Exclusion criteria

Exclusion criteria: 1. Patients with senile dementia and cognitive impairment before head injury; 2. Have mental or nervous system diseases, long-term use of sedative hypnotic drugs, opioids and psychotropic drugs; 3. Patients who are unable to communicate due to mental illness or hearing or vision impairment; 4. Patients admitted to intensive care unit after surgery.

Design outcomes

Primary

Measure	Time frame
Athens Insomnia Scale;	—

Countries

China

Contacts

Public ContactTan Wenfei

The First Hospital of China Medical University

winfieldtan@hotmail.com+86 24 8328 3100

Outcome results

None listed

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