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NCT06402357 · ClinicalTrials.gov registry record · Phase 2

High Intensity Focused Ultrasound in Prostate Cancer

A Phase 2 study of Prostate Cancer, sponsored by University of Florida.

Recruiting
Registry status
Phase 2
Development phase
25
Enrollment target
1
Study location

NCT06402357 is a Phase 2 study of Prostate Cancer that is actively recruiting participants, run by University of Florida. The registered enrollment target is 25 participants, below the 608-participant average among 735 other Prostate Cancer trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06402357, a Phase 2 study of Prostate Cancer, is actively recruiting participants, sponsored by University of Florida.

RECRUITING
Registry status
Phase 2
Development phase
25 participants
Enrollment target
1
Study location

Study Summary

This study will investigate the efficacy of focal high intensity focused ultrasound (HIFU) in patients with localized radiorecurrent prostate cancer. This study will also investigate the change in participant quality of life after HIFU therapy as compared to before HIFU therapy.

Conditions Studied

Prostate Cancer

Interventions

  • DEVICE Focal One high intensity focused ultrasound device

Study Locations (1)

Florida

  • University of Florida - Gainesville

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2025-05-14
Est. Completion 2029-08
Phase Phase 2

Sponsor

University of Florida

1,106 total trials

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What the Registry Record Tells You About NCT06402357

The ClinicalTrials.gov registry entry for NCT06402357 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 608-participant average among 735 other Prostate Cancer trials with a reported enrollment target (96% lower). The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Prostate Cancer appearing as the primary indexed condition, and to 1 intervention - of which Focal One high intensity focused ultrasound device is the first listed.

NCT06402357 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.

Frequently Asked Questions

What is clinical trial NCT06402357 about?

NCT06402357 is a clinical study titled "High Intensity Focused Ultrasound in Prostate Cancer". This study will investigate the efficacy of focal high intensity focused ultrasound (HIFU) in patients with localized radiorecurrent prostate cancer. This study will also investigate the change in participant quality of life after HIFU therapy as compared to before HIFU therapy.

What is the current status of trial NCT06402357?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 25 participants. The study started on 2025-05-14. Estimated completion is 2029-08.

What conditions does trial NCT06402357 study?

This clinical trial studies the following conditions: Prostate Cancer.

What interventions are being tested in trial NCT06402357?

The interventions under investigation include: Focal One high intensity focused ultrasound device (DEVICE).

Who is sponsoring clinical trial NCT06402357?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06402357 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.