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Life sciences · Interventional Study
ClinicalTrials.gov · September 17, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
No findings were extractable from the material analysed.
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 (NCT06362616). This is a study registration, not published results. Lead sponsor: The Netherlands Cancer Institute. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 31 participants (ESTIMATED). Conditions: Breast Cancer. Interventions: RADIATION: Preoperative accelerated partial breast irradiation; PROCEDURE: Breast conserving surgery; PROCEDURE: Sentinel node procedure; PROCEDURE: Biopsy track removal. Primary outcome measures: Acute post-treatment toxicity , 3,5 months. Brief summary: This study evaluates the acute toxicity and feasibility of repeat breast conserving therapy with preoperative accelerated partial breast re-irradiation (PAPBI) in female patients aged 51 years or older with ipsilateral recurrent or second primary low-risk breast cancer or DCIS.