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To evaluate the efficacy and feasibility of patient-reported outcome-based symptom management in patients undergoing radical prostatectomy: a prospective, multicenter clinical study

To evaluate the efficacy and feasibility of patient-reported outcome-based symptom management in patients undergoing radical prostatectomy: a prospective, multicenter clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082090
Enrollment
Unknown
Registered
2024-03-20
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Prostate Cancer

Interventions

Intervention group :Patient-reported outcomes-based symptom management
Control group:Routine symptom management

Sponsors

Lishui Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: ? Age 18 and above; ? Pathological diagnosis of prostate cancer; ? No cognitive impairment; ? Plan to undergo radical prostatectomy for prostate cancer.

Exclusion criteria

Exclusion criteria: ?Surgery cancellation; ?Patients who have been hospitalized in the ICU for more than 24 hours after surgery; ? Patients who have been hospitalized for more than 14 days after surgery; ? Patients with severe complications that impact data collection for assessment scales; ? Patients with postoperative pathological diagnosis of non prostate cancer; ? Intentionally providing incorrect data by patients; ? Patients who withdraw their informed consent form; ? The researcher assessed that it is not suitable to continue participating in this study.

Design outcomes

Primary

MeasureTime frame
Mean symptom threshold events;

Secondary

MeasureTime frame
Trajectories of MDASI Symptom Severity (Average Score of Five Target Symptoms);Trajectories of MDASI Daily Function (Average Score of Six Interference Items) ;Trajectories of Single item QoL scale (UNISCALE mean score);Unplanned revisit rate after discharge;

Countries

China

Contacts

Public ContactJie Li

Lishui Central Hospital

lijie9783@126.com+86 578 228 5218

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026