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RecruitingNCT07203482

Clinical Outcomes in Prostate Cancer Patients Undergoing HIFU Ablation

A Single-center Observational Study of Clinical Outcomes of Clinically Localized Prostate Cancer Undergoing HIFU Therapy

Status
Recruiting
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
NYU Langone Health · Academic / Other
Sex
Male
Age
40 Years – 95 Years
Healthy volunteers
Not accepted

Summary

Many reports of clinical outcomes following treatment of localized prostate cancer suffer from lack of prospective long-term data using objective and validated outcome instruments. The purpose of this research database is to prospectively collect data to assess treatment related complications, oncologic outcomes and urinary/sexual function, and identify predictors of complications, oncological control and functional outcomes after Hhigh-intensity focused ultrasound (HIFU) ablation of prostate cancer with the intent to guide further research and improve patient care. We will include subjects who will have a HIFU procedure performed from all Sub-Investigators included in the study.

Conditions

Timeline

Start date
2024-05-16
Primary completion
2030-12-31
Completion
2050-12-31
First posted
2025-10-02
Last updated
2025-10-02

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT07203482. Inclusion in this directory is not an endorsement.

Clinical Outcomes in Prostate Cancer Patients Undergoing HIFU Ablation (NCT07203482) · Clinical Trials Directory