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Prostate Ablation Registry and Database for Information, Surveillance, and Evaluation (PARADISE)
NCT06705803 · University of Chicago
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
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.
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 design
Enrollment target: 3000 participants
Age groups: adult, older_adult
Timeline
Starts: 2024-06-21
Estimated completion: 2029-06
Last updated: 2026-02-02
Interventions
Procedure: Prostate Ablation
Primary outcomes
- • Number of Participants with descriptive summarization of Prostate specific antigen (PSA) and its derivatives to represent clinicopathologic, interventions, and oncological outcomes (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 (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 (Follow up every 6 months (at minimum) for 2 years, and annually through 10 years of total follow-up after prostate cancer management.)
Sponsor
University of Chicago · other
With: University of Cincinnati
Contacts & investigators
ContactAbhinav Sidana, MD · contact · abhinav.sidana@bsd.uchicago.edu · 773-834-5087
ContactLeila Yazdanbakhsh · contact · leila.yazdanbakhsh@bsd.uchicago.edu · 773-834-5087
InvestigatorAbhinav Sidana, MD · principal_investigator, University of Chicago
All locations (2)
The University of ChicagoRecruiting
Hyde Park, Illinois, United States
The University of CinncinattiRecruiting
Cincinnati, Ohio, United States