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RECRUITING
NCT03620786

HIFU for Focal Ablation of Prostate Tissue: An Observational Study

Sponsor: University of California, Los Angeles

View on ClinicalTrials.gov

Summary

The Sonablate HIFU device was approved by the U.S.FDA for prostate tissue ablation in October, 2015. The purpose of this observational research study is to investigate the localized treatment of prostate cancer using HIFU through clinical data and health-related quality of life (HRQOL) questionnaires.

Official title: High-Intensity Focused Ultrasound for Focal Ablation of Prostate Tissue: An Observational Study of Multiparametric MRI and Ultrasound Fusion Imaging for Guidance

Key Details

Gender

MALE

Age Range

40 Years - 85 Years

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2018-09-26

Completion Date

2028-01-31

Last Updated

2025-03-13

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Sonablate HIFU device

In this study, we will be using the Sonablate 450 HIFU System. The Sonablate HIFU device was approved by the U.S. FDA for prostate tissue ablation in October, 2015. HIFU is an example of focal therapy, where the intervention involves targeting diseased areas of prostate tissue, while preserving healthy prostate tissue and minimizing damage to surrounding structures.

Locations (1)

University of California, Los Angeles

Los Angeles, California, United States