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Development of a new patient-reported outcome instrument for perioperative patient comfort

Development of a new patient-reported outcome instrument for perioperative patient comfort

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024334
Enrollment
Unknown
Registered
2019-07-06
Start date
2019-07-02
Completion date
Unknown
Last updated
2019-07-15

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

Conditions

Hospitalized perioperative patients

Interventions

Gold Standard:Clinical presentation and outcomes
Index test:patient-reported&#32

Sponsors

Department of anesthesiology, West China Hospital, Sichuan university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients>= 18 years old; 2. Patients received surgery under general anesthesia (including hepatic surgery, biliary tract surgery, pancreatic surgery, gastrointestinal surgery, plastic surgery, thyroid surgery, breast surgery, cardiac surgery, neurosurgery, orthopaedic surgery, thoracic surgery, urological surgery and ear-nose-throat surgery); 3. Patients with informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients can't understand the aim of the study and those with who can't communicate (including psychiatric patients and those in intubated status; 2. Patients received endoscopic surgery.

Design outcomes

Primary

MeasureTime frame
the reliability of the scale;the validity of the scale;

Countries

China

Contacts

Public ContactZuo Yunxia

West China Hospital, Sichuan University

76954913@qq.com+86 18980601541

Outcome results

None listed

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