Prostate Ablation Registry and Database for Information, Surveillance, and Evaluation (PARADISE)

Clinicaltrials.gov ID: NCT06705803
db-list-check Status RECRUITING
b-loader Phase
b-people Age ≥ 22 Years
b-bullseye-arrow Enrollments 3000

Conditions

Prostate Cancer

Summary

Prostate cancer (PCa) is the most commonly diagnosed non-cutaneous cancer of men in the world. In 2023 alone, it is estimated that 288,300 US men will be diagnosed with prostate cancer and 34,700 will die from the disease despite the approval of multiple systemic agents. Due to advances in screening and imaging technology, PCa is now detected much earlier in its disease course. Prostate gland ablation for prostate cancer might provide the option for a "middle" ground between active surveillance (AS) and radical therapy by destroying prostate cancer in a minimally invasive or non-invasive fashion and thus limiting the morbidity. This treatment strategy is increasingly being offered to patients due to low morbidity but the data on long term oncologic efficacy and side effect profile is lacking for such a treatment strategy.The purpose of this study is to create a database and prospective registry for data collection on patients with prostate cancer undergoing prostate ablation for the management of prostate cancer. Patients with biopsy-proven prostate cancer of any Gleason Grade will be entered into the registry as long as prostate ablation is used as the prostate cancer management modality. Historical data from 2017 to the present time will be added through chart review. Current and future patient data will be collected through chart review during the subject's clinical care. Only data available in the electronic medical record will be collected and no additional data will be collected for research purposes. No biospecimens will be collected, and there are no physical risks from study participation.

Locations

2 locations Found with status Recruiting

Status

  • RECRUITING

Contact Person

  • Abhinav Sidana, MD

Principal Investigator

  • Abhinav Sidana, MD

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Abhinav Sidana, MD

Eligibility Criteria

Inclusion Criteria:

* Male sex
* ≥22 years of age
* Histologic diagnosis of prostate cancer
* Scheduled to undergo or have already undergone ablation of the prostate as part of routine clinical care or any ongoing clinical trials
* Prostate ablation performed with any of the following energy sources: cryotherapy, high-intensity focused ultrasound, irreversible electroporation, laser, microwave, radiofrequency ablation, or photodynamic therapy. Newer methods and instrumentation continue to be developed to ablate tissue, and these energy sources can be entered into the registry as clinical use begins

Exclusion Criteria:

* Under 21 Years of age.

Study Plan

Prostate Cancer Patients Undergoing Prostate Ablation

Patients with prostate cancer undergoing prostate ablation for the management of prostate cancer.

  • PROCEDURE:

    Prostate Ablation

    Description:

    Patients with prostate cancer undergoing prostate ablation for the management of prostate cancer.

Outcome Measures

Primary Outcome Measures

Number of Participants with descriptive summarization of Prostate specific antigen (PSA) and its derivatives to represent clinicopathologic, interventions, and oncological outcomes

Time Frame: Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.

Number of Participants with descriptive summarization of prostate biopsy

Time Frame: Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.

Number of Participants with descriptive summarization of biomarkers

Time Frame: Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.

Number of Participants with descriptive summarization of imaging findings

Time Frame: Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.

Number of Participants with descriptive summarization of urination function

Time Frame: Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.

Number of Participants with descriptive summarization of bowel function

Time Frame: Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.

Number of Participants with descriptive summarization of sexual function

Time Frame: Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.

Number of Participants with descriptive summarization of the overall quality of life parameters

Time Frame: Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.

Secondary Outcome Measures

Incidence of Treatment-Emergent Adverse Events of prostate gland ablation in patients with localized prostate cancer measured on a continuous scale.

Time Frame: Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.

Timeline

  • Last Updated
    November 26, 2024
  • Start Date
    November 26, 2024
  • Today
    May 11, 2025
  • Completion Date ( Estimated )
    June 1, 2029

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