Clinical trial · Observational
Treatment Patterns Among Patients With Prostate Cancer Prior to Diagnosis of a Castration-resistant State
A Retrospective Observational Study to Describe Treatment Patterns Among Patients With Prostate Cancer Prior to Diagnosis of a Castration-resistant State, in Routine Clinical Practice in Spain.
NCT01560858CI-TRIAL-00036765completedClinicalTrials.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)
The purpose of the protocol is to describe treatment patterns among patients with prostate cancer prior to diagnosis of castration-resistant state.
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 (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (2)
- measure
- Prior treatment before progression to advanced or metastatic disease.
- timeFrame
- Baseline
- description
- Number of participants with each category of treatment.
- measure
- Treatment of advanced or metastatic disease.
- timeFrame
- Baseline
- description
- Number of participants with each category of treatment.
Secondary outcomes (4)
- measure
- Clinical management of Castration-Resistant Prostate Cancer (CRPC) patients in the clinical practice.
- timeFrame
- Baseline
- description
- Percentage of specialists (urologist, radiotherapist, oncologist or other specialist) in charge of treatment decision in CRPC patients.
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Age ≥ 18 years * Patients with prostate cancer who had developed a castration resistant state in the last 24 months prior to starting the study * Patient must give written informed consent before any study related procedure Exclusion Criteria: * Patients with medical histories lacking data required to evaluate the study objectives
References
Publications (0)
Data not yet available
No reference posted for this study.