Postoperative pain trajectory and its association with sleep quality in patients undergoing thoracoscopic pulmonary surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200062737

Enrollment

Unknown

Registered

2022-08-17

Start date

2022-08-15

Completion date

Unknown

Last updated

2023-04-12

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

Conditions

thoracoscopic pulmonary surgery

Interventions

Case series:None

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Aged>18; 2. Thoracoscopic pulmonary surgery.

Exclusion criteria

Exclusion criteria: 1. Unable to report pain intensity; 2. Without normal consciousness or cognitive function; 3. Postoperative ventilator support or intensive care; 4. Preoperative sleep disturbance; 5. Previous serious chronic diseases such as heart, liver, kidney, central nervous system, etc.; 6. Preoperative or long-term use of sedatives, antidepressants or drug dependence

Design outcomes

Primary

Measure	Time frame
postoperative sleep quality;	—

Secondary

Measure	Time frame
postoperative pain;	—

Countries

China

Contacts

Public ContactLinlin Zhao

lin1675@163.com+86 13685172831

Outcome results

None listed

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