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Hemi-Gland Cryoablation for Prostate Cancer at UCLA

Jonsson Comprehensive Cancer Center logo

Jonsson Comprehensive Cancer Center

Status

Invitation-only

Conditions

Prostate Disease
Prostate Adenocarcinoma
Prostate Cancer

Treatments

Device: Hemigland Cryoablation

Study type

Observational

Funder types

Other

Identifiers

NCT03503643
17-001084

Details and patient eligibility

About

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.

Enrollment

100 estimated patients

Sex

Male

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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