Establishment of a patient-reported assessment scale for the universality of postoperative recovery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000031624

Enrollment

Unknown

Registered

2020-04-05

Start date

2020-04-13

Completion date

Unknown

Last updated

2020-04-06

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

Conditions

None

Interventions

case series:N/A

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients over 18 years old; 2. ASA 1-3 patients; 3. Patients (excluding cardiac surgery and neurosurgery) who are hospitalized for surgery under selective general anesthesia; 4. Patients willing to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who are unable to communicate or understand the terms of this study 2. Patients with mental illness who have been treated with psychotherapy recently; 3. Patients unable to communicate due to complications, access to ICU or any other factors; 4. People who abuse drugs and alcohol.

Design outcomes

Primary

Measure	Time frame
length of stay;Pain VAS score;Physiological recovery;	—

Secondary

Measure	Time frame
Nausea and vomiting;Catheter related discomfort;	—

Countries

China

Contacts

Public ContactJin Liu

The West China Hospital of Sichuan University

scujinliu@foxmail.com+86 18980601539

Outcome results

None listed

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