Trial Comparing Prone and Supine Intensity-modulated Radiotherapy (IMRT) After Breast-conserving … (NCT00887523) | Clinical Trial Compass
CompletedNot Applicable
Trial Comparing Prone and Supine Intensity-modulated Radiotherapy (IMRT) After Breast-conserving Surgery in Patients With Large Breast Volume at High Risk for Skin Toxicity and Fibrosis
Belgium100 participantsStarted 2009-07
Plain-language summary
84 patients with a cup size C or more will be randomized to receive intensity-modulated radiotherapy in supine or prone position.
Who can participate
Age range18 Years
SexFEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* female patients
* multidisciplinary decision of adjuvant whole-breast irradiation (WBI) after lumpectomy for breast cancer
* minimum 18 years
* informed consent obtained, signed and dated before specific protocol procedures
Exclusion Criteria:
* mastectomy
* need for axillary irradiation
* bilateral breast irradiation
* previous irradiation at the same time
* mental condition rendering the patient unable to understand the nature, scope and possible consequences of the study
* patient unlikely to comply with the protocol; i.e. uncooperative attitude, inability to return for follow-up visits, and unlikely to complete the study.
What they're measuring
1
acute moist desquamation
Timeframe: weekly during radiotherapy and 1 month after radiotherapy