Clinical trial · Observational
Observational Study of Patients Who Underwent Diagnostic Investigation (Prostate Biopsy) and/or Radical Prostatectomy Surgery.
NCT06397755CI-TRIAL-00076720recruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a single-center, observational, prospective and retrospective study on quality of life and disease status of patients who underwent prostate biopsy and/or radical prostatectomy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Prostate Biopsy and/or Radical Prostatectomy | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Patients underwent prostate biopsy and/or radical prostatectomy surgery.
- interventionNames
- Procedure: Prostate Biopsy and/or Radical Prostatectomy
Primary outcomes (4)
- measure
- Clinically significant Prostate Cancer
- timeFrame
- 1 month
- description
- Diagnosis of clinically significant PCa at prostate biopsy
- measure
- Overall survival
- timeFrame
- every 6 month after surgery up to 50 years after surgery
- description
- Death by any cause
- measure
- Cancer-specific mortality
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients with a suspicious prostate disease who underwent prostate biopsy and/or radical prostatectomy; * Adult patients \> 18 years * Ability to read and sign the informed consent Exclusion Criteria: * Patients \< 18 years * mental or physical disability that may prevent the patient from satisfying the requirements of the protocol * Inability to read and sign the informed consent
References
Publications (0)
Data not yet available
No reference posted for this study.