Prostate Cancer Clinical Trial

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Hemi-Gland Cryoablation for Prostate Cancer at UCLA

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Summary

This is a prospective data collection of men who are electing to undergo prostate hemi-gland cryoablation.

The purpose of this observational research study is to investigate the localized treatment of prostate cancer using hemi-gland cryoablation.

UCLA patients undergoing hemi-gland cryoablation are a unique cohort compared to prior research because all patients at UCLA have had a pre-treatment multi-parametric MRI and Ultrasound fusion targeted biopsy; they will be followed in a similar fashion. This results in more precise assessment of a target region of cancer for ablation which may, in turn, result in improved clinical outcomes.

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Eligibility Criteria

Inclusion Criteria:

Patient has undergone or has elected to undergo hemi-gland cryoablation at UCLA
Low or intermediate risk prostate cancer (Gleason ≤ 7) or select high-risk patients (Gleason 8 prostate cancer).
Prostate volume of ≤ 70 cc
Ability to complete informed consent form

Exclusion criteria:

Medical contraindication to follow-up multi-parametric magnetic resonance imaging (mpMRI) or prostate biopsy
Patients unable to tolerate general or regional anesthesia.

Study is for people with:

Prostate Cancer

Estimated Enrollment:

100

Study ID:

NCT03503643

Recruitment Status:

Enrolling by invitation

Sponsor:

Jonsson Comprehensive Cancer Center

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There is 1 Location for this study

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University of California, Los Angeles
Los Angeles California, 90095, United States

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Study is for people with:

Prostate Cancer

Estimated Enrollment:

100

Study ID:

NCT03503643

Recruitment Status:

Enrolling by invitation

Sponsor:


Jonsson Comprehensive Cancer Center

How clear is this clinincal trial information?

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