Comparison of Intra-operative Radiotherapy With Post-operative Radiotherapy for Women With Early Breast Cancer

PHASE3CompletedINTERVENTIONAL
Enrollment

3,451

Participants

Timeline

Start Date

March 31, 2000

Primary Completion Date

June 30, 2012

Study Completion Date

June 30, 2012

Conditions
Invasive Breast CancerBreast Cancer
Interventions
DEVICE

Intrabeam

A dose of 20 Gy at the surface of the applicator or 6 Gy at 1cm (in water) is prescribed by the radiation oncologist and delivered to the breast tissue. This takes approximately 30 minutes, depending on the size of the applicator.

RADIATION

Post-operative radiotherapy

All patients randomised to receive conventional radiotherapy within this trial should be treated in accordance with a pre-specified policy. Dosage should only be applied to the breast; axillary, supra-clavicular and internal mammary nodes should not generally be irradiated by discrete fields.

Trial Locations (1)

N19 5LW

Clinical Trials Group, London

All Listed Sponsors
collaborator

National Institute for Health Research, United Kingdom

OTHER_GOV

lead

University College, London

OTHER

NCT00983684 - Comparison of Intra-operative Radiotherapy With Post-operative Radiotherapy for Women With Early Breast Cancer | Biotech Hunter | Biotech Hunter