UnknownNot Applicable

IORT-Boost-Study, Prospective Observational Study for Intraoperative Radiotherapy of the Breast as a Boost

Switzerland163 participantsStarted 2013-01

Plain-language summary

In this study the investigators observe the investigation, whether the new method for Boost-Irradiation with the Intrabeam Device of Zeiss Germany influences local recurrence, acute and late effects of Radiotherapy, overall survival, quality of life and cosmesis.

Who can participate

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: * women with histologically proven unifocal ductal-invasive or other histology of breast-cancer, size of tumor \< or = 3.5 cm * written informed consent * ability to cooperate * full legal capability Exclusion Criteria: * missing written informed consent * lack of compliance

What they're measuring

number of Participants with local recurrence histologically proven

Timeframe: up to 10 years

Trial details

NCT IDNCT02114086

SponsorKantonsspital Münsterlingen

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2019-12-31

View on ClinicalTrials.gov More Adverse Effect of Radiation Therapy trials