Clinical trial · Observational
A Long-term Observational Study Cohort in Patients With Advanced Prostate Cancer
A Prospective Observational Study Cohort to Assess the Rate of Castration Resistance, Disease Progression and Overall Survival Over a 3-year Period Post-androgen Deprivation Therapy Induction in Patients With Advanced Prostate Cancer Who Have Previously Participated in the Triptocare Study (Http://Clinicaltrials.Gov/ct2/Show/Study/NCT01020448)
- 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 assess the rate of castration resistance, disease progression and overall survival over a 3-year period post-androgen deprivation therapy (ADT) induction in a study cohort of patients with advanced disease.
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 |
|---|---|---|---|
| Advanced Prostate Cancer | Malignant Prostate Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Castration-resistant prostate cancer (CRPC)
- timeFrame
- Over a 3-year period post-androgen deprivation therapy induction
Secondary outcomes (4)
- measure
- Disease progression (DP) rate post-androgen deprivation therapy induction
- timeFrame
- Over a 3-year period post-androgen deprivation therapy induction
- measure
- Overall survival
- timeFrame
- 3-years post-androgen deprivation therapy induction
- measure
- Serum prostate specific antigen
- timeFrame
- Over a 3-year period post-androgen deprivation therapy induction
- measure
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Have participated and received study treatment in the Triptocare study * Be aware of the investigational nature of this observational study cohort and must give written (personally signed and dated) informed consent Exclusion Criteria: * Absence of written informed consent from the patient
References
Publications (0)
Data not yet available