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Clinical Trial Summary

Prospective, multicentric, comparative, non randomised, in current care. Primary objective: - To evaluate the incidence of hypothyroidism in breast cancer patients treated by radiotherapy including the supra-clavicular area over a period of 5 years (60 months). Secondary objectives : - To calculate the dose of irradiation received by thyroid gland during the treatment. - To compare the rate of incidence of hypothyroidism in women who received a supra-clavicular irradiation (group 1)and in those who did not (group 2). - To estimate and compare the rate of incidence of chronic thyroid lesions in the 2 groups. - To look for predictive factors of hypothyroidism de novo in group 1 women particularly regarding the dose-volume parameters. - To propose recommendations for the thyroid follow-up after supra-clavicular irradiation.


Clinical Trial Description

Prospective, multicentric, comparative, non randomised, in current care study 2 patient groups, non randomised, according to the necessity or not to perform a supra-clavicular irradiation: - Group 1 : patients receiving a supra-clavicular irradiation - Group 2 : patients not receiving a supra-clavicular irradiation. Schedule Projected inclusion duration of 18 months (duration to possibly adapt in order to obtain the number of required patients) Intermediate study of the results in 30 months Duration of follow-up of 60 months ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02824016
Study type Interventional
Source Institut Jean-Godinot
Contact
Status Completed
Phase N/A
Start date February 2013
Completion date July 2020

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