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Spots Global Cancer Trial Database for Phase 3, Multicenter, Randomized Study, Evaluating the Efficacy and Tolerability of Focused HIFU (High Intensity Focused Ultrasound) Therapy Compared to Active Surveillance in Patients With Significant Low Risk Prostate Cancer

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Trial Identification

Brief Title: Phase 3, Multicenter, Randomized Study, Evaluating the Efficacy and Tolerability of Focused HIFU (High Intensity Focused Ultrasound) Therapy Compared to Active Surveillance in Patients With Significant Low Risk Prostate Cancer

Official Title: Phase 3, Multicenter, Randomized Study, Evaluating the Efficacy and Tolerability of Focused HIFU Therapy Compared to Active Surveillance in Patients With Significant Low Risk Prostate Cancer

Study ID: NCT03531099

Conditions

Prostate Cancer

Study Description

Brief Summary: The percentage of malignant prostate tumors detected very early is constantly increasing and the number of well differentiated tumors, with small volume and low risk of progression increases. When a tumor of this type is identified, radical prostatectomy remains the reference treatment, but this treatment is not without side effects. Active surveillance is a strategy which aims at detecting an early development of the cancerous disease in order to propose curative treatment in a timely manner and thus improve specific survival. Patients are therefore re-evaluated each year by rectal examination, PSA (Prostate-Specific Antigen) assay. Active surveillance remains difficult to manage psychologically for both the patient and the practitioner, because of the lack of treatment on the one hand and a rate of non-curable cancers close to 50% when signs of progression trigger a radical treatment. The aim of the focal treatment HIFU (High Intensity Focused Ultrasound) is to destroy the cancer without causing side effects in contrast to radical treatments. It is in this sense that it is positioned both as an alternative to radical surgery and as an alternative to active surveillance.

Detailed Description:

Eligibility

Minimum Age: 50 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Polyclinique du parc Rambot, Aix-en-Provence, , France

Clinique Saint-Vincent, Besançon, , France

Service d'Urologie, Clinique Tivoli Ducos, Bordeaux, , France

Groupe Hospitalier Pellegrin - CHU, Bordeaux, , France

Service d'Urologie, CHU de Guebwiller Colmar, Colmar, , France

Service d'Urologie CHRU de Lille, Hôpital HURIEZ, Lille, , France

Service d'Urologie Générale de Santé - Hôpital Privé La Louvière, Lille, , France

Service d'Urologie et Chirurgie de la Transplantation, Hôpital Edouard Herriot,, Lyon, , France

Service d'urologie Assistance Publique - Hôpitaux de Marseille - Hôpital Marseille Nord, Marseille, , France

Département d'Urologie, Institut Montsouris, Paris, , France

Centre Hospitalier Lyon Sud, Pierre-bénite, , France

Clinique Urologique Nantes Atlantis, Saint-Herblain, , France

Service d'Urologie, Hôpital Foch, Suresnes, , France

CHU de Toulouse - Hôpital de Rangueil, Toulouse, , France

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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