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Reliability and validity test and utility parameters development of a patient-reported outcome (PRO)-based perioperative symptom scale for lung cancer patients (CN-PRO-Lung 3)

A study to establish a dynamic recovery cohort of lung cancer patients in perioperative period based on patient-reported outcomes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033016
Enrollment
Unknown
Registered
2020-05-18
Start date
2020-09-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

lung cancer

Interventions

Sponsors

Sichuan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who are initially diagnosed with primary lung cancer and scheduled to undergo surgery.

Exclusion criteria

Exclusion criteria: Patients who are aged < 18 years or have cognitive impairment.

Design outcomes

Primary

MeasureTime frame
lung cancer perioperative symptom scale;utility parameters;

Countries

China

Contacts

Public ContactShi Qiuling

Sichuan Cancer Hospital

qshi@cqmu.edu.cn+86 182 9058 5397

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026