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Clinical Trial Summary

This trial is a multicenter, perspective, non-blinded, randomized controlled phase 3 trial. In order to establish whether the SIB technique can improve the results of twice-daily chemo-RT for patients with LS-SCLC, the investigators will primarily compare survival of patients treated with standard chemotherapy (cisplatin and etoposide) and either SIB twice-daily RT or standard dose twice-daily RT.


Clinical Trial Description

Three hundred and twenty-six patients with a histological or cytological proven diagnosis of SCLC will be recruited from 35 centers in 14 areas including provinces, municipalities and autonomous region, from May 2017 to May 2020. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03214003
Study type Interventional
Source Peking University Cancer Hospital & Institute
Contact
Status Completed
Phase N/A
Start date June 30, 2017
Completion date January 30, 2023

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