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Fibroadenoma clinical trials

View clinical trials related to Fibroadenoma.

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NCT ID: NCT03022695 Completed - Breast Fibroadenoma Clinical Trials

Treatment of Breast Fibroadenoma With High Intensity Focused Ultrasound (HIFU)

HIFU
Start date: October 2013
Phase: N/A
Study type: Interventional

This is a monocenter, open-label, uncontrolled study in accordance with §23b MPG to evaluate the efficacy of the HIFU-treatment of fibroadenoma using the TH-One device.

NCT ID: NCT02488655 Completed - Breast Fibroadenoma Clinical Trials

Treatment of Breast Fibroadenoma With FastScan HIFU

Start date: June 2015
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of the HIFU for the treatment of breast fibroadenoma with the FastScan version using assessment of patient experience and adverse event reporting.

NCT ID: NCT02139683 Completed - Breast Fibroadenoma Clinical Trials

Feasibility Study Assessing the Treatment of Fibroadenomata With a Circumferential Sonication Treatment With HIFU

Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the treatment of fibroadenomata with a circumferential sonification treatment with HIFU..

NCT ID: NCT02078011 Completed - Breast Fibroadenoma Clinical Trials

Treatment of Breast Fibroadenoma With High Intensity Focused Ultrasound

HIFU-FA-001
Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to test an investigational device called the Echopulse for treatment of breast fibroadenomas in women. Fibroadenomas are benign (noncancerous) breast tumors that are made of glandular and fibrous breast tissue. These lumps can occur alone, in groups, or as a complex of lumps together. Sometimes women feel these in the breast when doing regular self breast exams, or they may be found during a routine mammogram. Some are small (less than an inch in size), and others are quite large (the size of a lemon or larger). This is a study about the Echopulse device, a computer driven system which uses ultrasound to guide a high intensity focused ultrasound beam to a targeted area (the fibroadenoma in the breast). The high intensity focused ultrasound (HIFU) heats the targeted site which causes the cells to die and allows the possibility to treat the fibroadenoma without the need for surgery.

NCT ID: NCT02011919 Completed - Breast Fibroadenoma Clinical Trials

Treatment of Breast Fibroadenoma With High Intensity Focused Ultrasound (HIFU)

HIFU
Start date: December 2013
Phase: N/A
Study type: Interventional

This is a monocenter, open-label, uncontrolled study in accordance with §23b MPG to evaluate the efficacy of the HIFU-treatment of fibroadenoma using the TH-One device Objectives Primary objective: To evaluate the efficacy of HIFU in the treatment of the breast fibroadenoma using the TH-One device Secondary objective: To evaluate the tolerability of the HIFU using the TH-One device

NCT ID: NCT01422629 Completed - Breast Fibroadenoma Clinical Trials

High Intensity Focused Ultrasound (HIFU) to Treat Breast Fibroadenoma

Start date: October 2011
Phase: N/A
Study type: Interventional

This study is a multicentre, open, uncontrolled trial for the observation of histological changes in breast fibroadenoma following high intensity focused ultrasound (HIFU). This study will be conducted in France in 20 patients with breast fibroadenoma with indication for a surgical resection. The patient will receive an HIFU treatment and 6 months after treatment, the need of the surgery is evaluated.

NCT ID: NCT01331954 Active, not recruiting - Breast Fibroadenoma Clinical Trials

Treatment of Breast Fibroadenoma With High Intensity Focused Ultrasound (HIFU)

Start date: March 2011
Phase: N/A
Study type: Interventional

Demonstrate the efficacy of High Intensity Focused Ultrasound in the treatment of the breast fibroadenoma.

NCT ID: NCT00999921 Completed - Clinical trials for Benign Breast Disease

Effects of Tamoxifen in Premenopausal Women With Benign Breast Disease Not at High-Risk of Developing Breast Cancer

Start date: January 2008
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine the efficacy and relapse rate of low dose, short duration treatment with tamoxifen in benign breast disease amenable to hormonal therapy with respect to etiology and estrogen receptor status and to realize its side-effects and cost of therapy. To do a comparative analysis of the results with evening primrose oil which is one of the first line management in benign breast disease.

NCT ID: NCT00910312 Completed - Fibroadenoma Clinical Trials

ICE-SENSEā„¢ Cryotherapy for Breast Fibroadenoma Trial

ICE-CRYSTAL
Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the Ice-Sense, a novel cryotherapy system (a system that freezes tissues), is safe and effective in the treatment of benign breast tumors such as fibroadenoma.

NCT ID: NCT00807924 Completed - Clinical trials for Benign Breast Conditions; Breast Fibroadenomas

American Breast Laser Ablation Therapy Evaluation

ABLATE
Start date: December 2008
Phase:
Study type: Observational

The purpose of this patient tracking program is to monitor long term safety and effectiveness of the Novilaseā„¢ device and method in real world application.