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NSABP PROTOCOL B-39: ADVERSE EVENT FORM FOR RADIATION THERAPY NCT00103181 Radiation Therapy in Treating Women Who Have Undergone Surgery For Ductal Carcinoma In Situ or Stage I or Stage II Breast Cancer Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=E6F7DDC5-C879-6CDA-E034-0003BA3F9857

Link:
https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=E6F7DDC5-C879-6CDA-E034-0003BA3F9857
Palavras-chave:
  1. 26/08/2012 26/08/2012 -
  2. 08/01/2015 08/01/2015 - Martin Dugas
  3. 08/06/2015 08/06/2015 -
Transferido a:

8 de junho de 2015

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Licença :
Creative Commons BY-NC 3.0 Legacy
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NSABP PROTOCOL B-39: ADVERSE EVENT FORM FOR RADIATION THERAPY NCT00103181

This paper worksheet may be completed to facilitate the entry of the adverse event information in NSABP Coordinator Online. Partially completed forms may be saved in Coordinator Online. DO NOT SUBMIT THIS WORKSHEET VIA FAX OR MAIL. For Protocol B-39, Form AE collects only adverse events that are possibly, probably, or definitely related to whole breast irradiation (WBI) or partial breast irradiation (PBI), regardless of whether these adverse events are expected or unexpected. Do not report adverse events resulting from chemotherapy, hormonal therapy or any other systemic cancer therapy. Complete Form AE at the end of each Reporting Period, as defined below. The Reporting Period Start Date should not lapse or overlap with the Reporting Period End Date of the prior Form AE. If the patient has a breast cancer recurrence or second primary cancer, please use the date of the cancer event as the reporting period end date. No additional AE forms will be required for this patient. If patient did not start RT, do not submit Form AE. If patient started radiation therapy (RT), use Form AE to report adverse events that are POSSIBLY, PROBABLY, or DEFINITELY RELATED to radiation therapy.

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Are data amended? (check box if yes, and circle amended items)
Reporting Period
Reporting period
Was patient hospitalized for 24 hours or more?
Grade
Ii. Infections
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