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

Kantonsspital Münsterlingen

Status: Active, not recruiting

Conditions: Adverse Effect of Radiation Therapy

Study type: Observational

Funder types: Other

Identifiers

NCT02114086

ROKSM 01/12

KMünsterlingen (Other Identifier)

Details and patient eligibility

About

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.

Enrollment: 163 patients

Sex: Female

Volunteers: No Healthy Volunteers

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

Trial design

163 participants in 1 patient group

breast cancer

Description:

observation of intraoperative radiotherapy