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Life sciences · Observational Study
ClinicalTrials.gov · September 21, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Observational Study.
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Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT07338721). This is a study registration, not published results. Lead sponsor: Antalya Training and Research Hospital. Recruitment status: COMPLETED. Study type: OBSERVATIONAL. Enrollment: 100 participants (ACTUAL). Conditions: Breast Carcinoma, Sentinel Lymph Node Biopsy. Interventions: PROCEDURE: Ultrasound-guided axillary incision group; PROCEDURE: The standard axillary incision. Primary outcome measures: Intraoperative assessment of surgical performance parameters. , Until completion of the sentinel lymph node procedure. Brief summary: This single-center randomized controlled trial evaluates whether detecting the first lymph node at the axillary entrance with ultrasound guidance, followed by a targeted axillary incision over the pencil-marked projection, improves sentinel lymph node identification compared to the conventional axillary hairline landmark. The study hypothesizes that this technique enables a smaller incision, minimizes tissue dissection, and reduces operative time.