UnknownNot Applicable

Quality of Life and Cosmetic Outcomes of Breast-Conserving Surgery According to Localization Method

Spain150 participantsStarted 2023-10-04

Plain-language summary

The goal of this clinical trial is to compare Quality of Life and cosmetic outcomes in Breast Conservative Carcer surgery depending on localization method (intraoperative Ultrasound, wire and radioactive seed). Participants will be randomly assigned to one of the three proposed arms, and the primary surgery will be performed.

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients diagnosed with non-palpable and ecovisible infiltrating breast carcinoma, classified as T1 and T2, eligible for primary breast-conserving surgery (BCS) Exclusion Criteria: * lesions \<5mm * multicentric tumors * extensive calcifications not visible by ultrasound * level III oncoplastic techniques or mastectomy

What they're measuring

BCCT.core

Timeframe: 12 months after surgery

BREAST-Q questionnaire

Timeframe: preoperative, 12 months after surgery

Trial details

NCT IDNCT06186011

SponsorHospital Clinic of Barcelona

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-10

Contact for this trial

Eduard Mension, MD PhD

+34 626207171 edmension@gmail.com

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