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Study identifier: NCT07206121 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Feasibility Study for the SIRA-1000, SIRA® RFA Electrosurgical Device as an Adjunct to Breast Conserving Surgery

Condition: Breast Cancer · Breast-conserving Surgery · Breast Cancer - Infiltrating Ductal Carcinoma  ·  Sponsor: Innoblative Designs, Inc.

PhaseNA
Planned participants10
Who can joinFemale, 50 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to assess the safety and clinical accuracy of the SIRA-1000, SIRA® RFA Electrosurgical Device in ablating margins post-lumpectomy in patients undergoing breast conserving surgery for breast cancer. Radiofrequency ablation, or RFA, uses radio waves to create heat, that in turn, causes deliberate controlled damage to the tissue surrounding where the tumor was located. You may hear your doctor refer to this as the 'margins'. Your doctor is using this treatment to help destroy remaining cancer cells in the margins around the site of the lump.

This description comes directly from the study's public registry record.

Talk to the study team

Clinical Trials Manager  ·  833-920-4660  ·  kathy@innoblative.com

VP Quality Assurance & Regulatory Affairs  ·  833-920-4660  ·  kcrowley@innoblative.com

Always discuss trial participation with your own doctor first.

Locations (1)

University of Texas Medical Branch at Galveston, TXGalveston, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07206121