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TARGeted Intraoperative radioTherapy With INTRABEAM as a Boost for Breast Cancer - A Quality Control Registry

NCT01440010 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1133

Last updated 2025-12-12

Study results available
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Summary

Quality Control Registry for IORT used as an anticipiated boost with 20 Gy at the applicator surface followed by EBRT

Conditions

Interventions

RADIATION

IORT with 20 Gy

Intraoperative radiotherapy with the INTRABEAM System with 20 Gy

Sponsors & Collaborators

  • Universitätsmedizin Mannheim

    lead OTHER

Principal Investigators

  • Elena Sperk, MD · Universitätsmedizin Mannheim

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-09-01
Primary Completion
2020-12-31
Completion
2020-12-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01440010 on ClinicalTrials.gov