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Reliability and validity test and utility parameters development of an electronic patient-reported outcome (PRO)-based perioperative symptom scale for gynecologic malignancies patients: a multicentre, prospective, observational cohort study (CN-PRO-Gynecologic Malignancies 3)

A longitudinal study based on electronic patient-reported outcomes after gynecologic malignancies surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114457
Enrollment
Unknown
Registered
2025-12-12
Start date
2025-12-15
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Gynecologic malignancies

Interventions

reliability and validity verification:None
Longitudinal cohort study:None

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
14 Years to 80 Years

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: Patients who are aged < 14 years or have cognitive impairment, nable to complete the scale.

Design outcomes

Primary

MeasureTime frame
Gynecological cancer perioperative symptom scale;—

Secondary

MeasureTime frame
Progression-free survival;Overall Survival;Interval of anti-tumor treatment;—

Countries

China

Contacts

Public ContactQu Dacheng

Affiliated Hospital of North Sichuan Medical College

qdc3253859@163.com+86 138 9074 5770

Outcome results

None listed

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