Focal Therapy for Localized Prostate Cancer

Clinicaltrials.gov ID: NCT06270043
db-list-check Status RECRUITING
b-loader Phase
b-people Age ≥ 18 Years
b-bullseye-arrow Enrollments 500

Conditions

Prostate Cancer

Summary

This prospective registry and longitudinal study that is designed to carefully measure details of prostate cancer patients' outcomes with focal therapy. The goal of which is to improve patient care.

Detailed Description

This observational study will serve to collect data from medical record and review questionnaires before and after focal ablation of prostate tissue. All enrolled subjects will have already undergone or scheduled to receive the focal therapy as part of their prostate cancer treatment.

Locations

1 location Found with status Recruiting

Status

  • RECRUITING

Contact Person

Eligibility Criteria

Inclusion Criteria:

* Subject has elected or already undergone focal therapy as their standard of care treatment method and declined alternative treatment (active surveillance, radical prostatectomy, and radiation therapy)
* PSA ≤ 20
* Ability to complete informed consent form

Exclusion Criteria:

* Contraindication to follow-up multi parametric MRI or prostate biopsy
* Unable to tolerate general or regional anesthesia

Study Plan

Focal Therapy

Subjects who have biopsy-proven adenocarcinoma of the prostate, who have met all study inclusion and exclusion criteria, and have elected to receive or have already received focal therapy as part of their routine prostate cancer treatment, will be invited to participate in this observational registry study.

  • PROCEDURE:

    Focal Therapy

    Description:

    Focal ablation of prostate cancer using different modalities. These modalities include:nn* Cryoablation or Cryotherapyn* Irreversible Electroporation - Nanoknifen* High Intensity Frequency Ultrasound - FocalOnen* Transurethral Ultrasound Ablation - TULSA - PRO

Outcome Measures

Primary Outcome Measures

Oncological Response

Time Frame: 1 year

Secondary Outcome Measures

Erectile Dysfunction

Time Frame: 1 year

Incontinence

Time Frame: 1 year

Prostate cancer recurrence. Patients will be monitored with a Prostate Specific Antigen (PSA) every 6 months until 10 years from the intervention. Patients with a rising PSA will receive a prostate biopsy to determine if they have a recurrence.

Time Frame: 10 years

Timeline

  • Last Updated
    February 26, 2024
  • Start Date
    February 21, 2024
  • Today
    February 5, 2025
  • Completion Date ( Estimated )
    February 1, 2034

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