Study reveals best Surgery-Radiation combos for Better-Looking breasts after cancer
NCT ID NCT05263362
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study involved 775 women who had breast-conserving surgery and radiation for breast cancer. Researchers compared different surgery and radiation techniques to see which ones led to less breast hardening (fibrosis) and better cosmetic results. The goal was to find ways to improve how the breast looks and feels after treatment, helping women feel better about their appearance and quality of life.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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775 people
The number who actually took part.
- Started
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Apr 2022
- Finished
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Sep 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consists of breast cancer patients who were treated with breast conserving therapy (BCT) at one of the four participating hospitals (Erasmus MC, Albert Schweitzer hospital, Maasstad hospital and Franciscus hospital Gasthuis and Vlietland), for non-metastatic, histological proven invasive breast cancer or DCIS between 2016 and 2020 (at time of inclusion in 2022 respectively 6 to 2 years after treatment), and subsequently received adjuvant radiotherapy of the whole breast at the Erasmus MC as part of their BCT.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Female patients aged ≥ 18 years * History of BCT with adjuvant radiation therapy for non-metastatic, histologically proven invasive breast cancer or DCIS. In light of BCT adjuvant systemic treatment (i.e. endocrine therapy, chemotherapy and immune therapy) is allowed. * Operated between 1st of January 2016 and 31th of December 2020 * Treated according to the currently applied dose fractionation schedules, i.e. whole breast radiotherapy (22, 23), with or without boost * Adequate understanding of the Dutch language and written informed consent Exclusion Criteria: * Any breast surgery or re-irradiation on the breast area after BCT * Progression of disease (and additional treatment) since BCT * Patients who received partial breast irradiation * Current pregnancy or breast feeding
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Albert Schweitzer hospital
Dordrecht, Netherlands
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Erasmus Medical Center
Rotterdam, Netherlands
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Franciscus Gasthuis & Vlietland
Schiedam, Netherlands
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Maasstad hospital
Rotterdam, Netherlands
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Other studies related to the condition(s) this trial covers.
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