Fact CheckerSign in

NCT06473259Recruiting

Evaluation of Clinical Outcomes of Chemotherapy or Androgen-receptor Targeting Agent (Alone or Combined) or Radiotherapy on Primary Tumor in Addition to Androgen Deprivation Therapy in HOrmone-Sensitive Metastatic Prostate Cancer Patients

Evaluation of Clinical Outcomes of Chemotherapy or Androgen-receptor Targeting Therapy (Alone or in Combination) or Radiotherapy on the Primary Tumor in Combination With Androgen Deprivation Therapy in Metastatic Hormone-sensitive Prostate Cancer: Multicenter Observational Study of Patients Undergoing Treatment in Clinical Practice in Italian Hospitals

Source: ClinicalTrials.gov · Last updated 25 Jun 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The aim of this observational study is to evaluate the clinical outcomes of treatment with docetaxel, ARTA (alone or in combination) or with radiotherapy on the primary tumor for mCSPC, in an unselected population, in clinical practice

Status (registry)
Recruiting
Study type
Observational
Enrollment
3000 (estimated)
First submitted
28 May 2024
Start date
16 Dec 2016
Primary completion date
Dec 2026
Lead sponsor
Santa Chiara Hospital
NCT number
NCT06473259

What you commit to

  • Study type: Observational
  • Planned participants: 3000
  • From 16 Dec 2016 to the primary completion date, Dec 2026
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • patients who have received multiple lines of ADT for mCSPC
  • patients who have received docetaxel or ARTA for metastatic castration-resistant disease

Other

  • histological diagnosis other than adenocarcinoma

Who the study is looking for

  • histologically confirmed diagnosis of adenocarcinoma of the prostate, metastatic, not undergoing previous treatment (except hormone therapy initiated no more than 4-6 months prior to docetaxel) for metastatic disease
  • treatment with docetaxel, ARPI (alone or in combination) or with radiation therapy on the primary tumor in combination with ADT within normal clinical practice or expanded access programs initiated between January 2015 and December 2027.
  • availability of inpatient and/or outpatient medical records for clinical data collection

Sex: Male

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Azienda Ospedaliera San Luigi
Coordinator of this site? Confirm its status
OrbassanoItalyRecruiting
Istituto Oncologico Veneto
Coordinator of this site? Confirm its status
PadovaItalyRecruiting
Santa Chiara Hospital
Coordinator of this site? Confirm its status
TrentoItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.