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Clinical Trial

Water Vapor Ablation for Grade Group 3 Prostate Cancer

NCT: NCT07652164 · NOT_YET_RECRUITING

NCT IDNCT07652164
StatusNOT_YET_RECRUITING
Start Date2026-08-31
SponsorFrancis Medical Inc. (INDUSTRY)
First posted
Last updated

Brief Summary

The goal of this study is to evaluate the safety and effectiveness of the Vanquish Water Vapor Ablation System ("Vanquish") in participants with Grade Group 3 (GG3) intermediate-risk prostate cancer. Participants will undergo therapy with the Vanquish System and complete follow up visits at 7 days, 6 weeks, 6 months, 12 months, 18 months, and 24 months.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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