Establishment and verification of perioperative delirium intervention strategy for patients undergoing thoracic surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000038038

Enrollment

Unknown

Registered

2020-09-09

Start date

2021-03-01

Completion date

Unknown

Last updated

2022-06-20

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

Conditions

Postoperative delirium

Interventions

Experimental group:perioperative delirium intervention strategy for patients undergoing thoracic surgery

control group:conventional care supported by the routine technique

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients with elective thoracic surgery; 2. The estimated anesthetic time is more than 2 hours; 3. Agree to the experimental scheme and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Inability to communicate before surgery (coma, severe dementia, language impairment); 2. Participated in other clinical trials within 3 months before the study was enrolled; 3. Patients who did not have the operation for any reason

Design outcomes

Primary

Measure	Time frame
Postoperative delirium;	—

Secondary

Measure	Time frame
delayed neurocognitive recovery;Postoperative pain score;Postoperative delirium severity;Duration of postoperative delirium;Classification of postoperative delirium;	—

Countries

China

Contacts

Public ContactJing Yang

West China Hospital, Sichuan University

hxyangjing@qq.com+86 18980602269

Outcome results

None listed

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