Dosimetric Comparison of Doses in Both Positions (Prone and Decubitus) for Patient With Breast Cancer

NCT ID: NCT02704312

Last Updated: 2022-03-08

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 11 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-11-30
• Study Completion Date: 2022-02-11

Brief Summary

Compare dosimeters in both positions (prone and decubitus) for each patient

Detailed Description

Quantitative Physics: dosimetric comparison of doses in target volumes and organs at risk. The technique used is that of which the dose on the organs at risk is as low as possible, and whose dose to the target volume is the closest possible to the prescribed dose (100% of the prescribed dose).

Conditions

Breast Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Radiotherapy techniques

Quantitative Physics: dosimetric comparison of doses in target volumes and organs at risk. The technique used is that of which the dose on the organs at risk is as low as possible, and whose dose to the target volume is the closest possible to the prescribed dose (100% of the prescribed dose)

Group Type: EXPERIMENTAL

Radiotherapy by Prone and decubitus

Intervention Type: RADIATION

Dosimetric comparison of doses in target volumes and organs at risk

Interventions

Radiotherapy by Prone and decubitus

Dosimetric comparison of doses in target volumes and organs at risk

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

• Patients with primary breast cancer and in whom conservative post- surgery radiation therapy for breast cancer is prescribed.
• Patients aged over 18 years
• Patients with indication for conservative surgery.
• Resection should be in healthy margin.
• Women of childbearing potential must satisfy a negative pregnancy test at the screening visit and use effective contraception as determined by the physician of the patient throughout the study.

Exclusion Criteria

• Minor Patient
• Patients whose tumor resection is incomplete
• Patients with an indication of mastectomy
• Patients with a history of radiation therapy of the chest
• Pregnant women, lactating, or of childbearing age without effective contraception.
• Patients who had more than 4 scanners in one year. ( Scanner cervical , thoracic, or abdominal
• Patients with an incompatible condition with monitoring protocol (psychiatric disorder, uncontrolled disease).
• Patient unable to respond to a questionnaire

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

University Hospital Center of Martinique

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Vincent VINH HUNG, MD

Role: PRINCIPAL_INVESTIGATOR

CHU de Martinique

Locations

CHU de Martinique

Fort-de-France, , Martinique

Countries

Martinique

Other Identifiers

15/ B/ 25

Identifier Type: -

Identifier Source: org_study_id