Skip to content

Developing and validating utility parameters to establish patient-reported outcome-based perioperative symptom management in patients undergoing prostatectomy: a prospective, observational cohort study

A study for perioperative symptom management in patients with prostate cancer based on patient-reported outcomes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200059110
Enrollment
Unknown
Registered
2022-04-25
Start date
2023-04-27
Completion date
Unknown
Last updated
2024-02-11

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

Conditions

Prostate cancer

Interventions

case series:None

Sponsors

Lishui Municipal Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: Aged >=18 years, no cognitive impairment or understanding of study requirements, preoperative pathological diagnosis of primary prostate cancer, and planned surgical treatment.

Exclusion criteria

Exclusion criteria: 1. Cancel the planned operation; 2. Postoperative tracheal intubation in intensive care unit for more than 24 hours; 3. Postoperative hospital stay more than 14 days; 4. Failure to comply with the research protocol (intentionally providing incorrect PRO data); 5. Withdrawal from the study or other circumstances that require withdrawal as assessed by the investigator.

Design outcomes

Primary

MeasureTime frame
prostate cancer perioperative symptom scale;

Secondary

MeasureTime frame
utility parameters;

Countries

China

Contacts

Public ContactLi Jie

Lishui Municipal Central Hospital

lijie9783@126.com+86 159 9084 8220

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026