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NCT07860528Recruiting

Study on Prostate Salvage Using High-dose-rate Brachytherapy

Multicenter Prospective Observational Study on Prostate Salvage Using High-dose-rate Brachytherapy

Source: ClinicalTrials.gov · Last updated 9 Oct 2026

Brief summary (registry, in English)

A prospective, observational, multicenter study analyzing salvage treatment for prostate cancer-diagnosed via next-generation imaging (choline positron emission tomography (PET)/prostate-specific membrane antigen (PSMA) PET and magnetic resonance imaging (MRI)) and positive biopsy-using two fractions of high-dose-rate (HDR) brachytherapy.

Status (registry)
Recruiting
Study type
Observational
Enrollment
63 (estimated)
First submitted
30 Sept 2026
Start date
11 Mar 2026
Primary completion date
31 Jan 2032
Lead sponsor
Instituto de Investigación en Oncología Radioterápica - Fundación Española de Oncología Radioterápic
NCT number
NCT07860528

What you commit to

  • Study type: Observational
  • Planned participants: 63
  • From 11 Mar 2026 to the primary completion date, 31 Jan 2032
  • 10 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.

Other illness

  • Metastatic disease.
  • Castration-resistant prostate cancer, defined according to EAU (European Association of Urology) guidelines: A patient who progresses despite maintaining testosterone levels within the castration range (testosterone \<50 ng/dL or \<1.7 nmol/L) and presents with at least one of the following factors: Three consecutive rises in PSA (Prostate-Specific Antigen) levels, measured one week apart, representing two increases of 50% above the nadir, with a PSA level \>2; PSA progression despite successive hormonal manipulations; Progression of bone lesions: progression or appearance of two or more bone lesions, or soft-tissue progression according to Response Evaluation Criteria in Solid Tumors (RECIST criteria).

Who the study is looking for

  • Age over 18 years.
  • Patients diagnosed with local recurrence confirmed by next-generation imaging and a positive biopsy.
  • Hormone-sensitive patient.
  • Patients whose initial treatment consisted of brachytherapy alone, external beam radiotherapy, or external beam radiotherapy with a prostate brachytherapy boost.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

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

SiteCityCountrySite status
Hospital Universitario de Cruces
Coordinator of this site? Confirm its status
BarakaldoSpainNot yet recruiting
Hospital HCB Benidorm
Coordinator of this site? Confirm its status
BenidormSpainRecruiting
Hospital Universitario Reina Sofia
Coordinator of this site? Confirm its status
CórdobaSpainRecruiting
Instituto Catalán de Oncología L'Hospitalet
Coordinator of this site? Confirm its status
L'Hospitalet de LlobregatSpainRecruiting
Hospital Universitario Ramón y Cajal
Coordinator of this site? Confirm its status
MadridSpainRecruiting
Hospital Universitario de Navarra
Coordinator of this site? Confirm its status
PamplonaSpainRecruiting
Instituto Oncológico de San Sebastián (Onkologikoa)
Coordinator of this site? Confirm its status
San SebastiánSpainNot yet recruiting
Hospital Universitario Marqués de Valdecilla
Coordinator of this site? Confirm its status
SantanderSpainRecruiting
Hospital Universitario Y Politecnico La Fe
Coordinator of this site? Confirm its status
ValenciaSpainRecruiting
Hospital Meixoeiro
Coordinator of this site? Confirm its status
VigoSpainRecruiting

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