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Clinical Trial Summary

The purpose of this non-interventional study is to collect data on the risk factors for acute radiation pneumonitis in patients with prior receipt of immune checkpoint inhibitors.


Clinical Trial Description

1. Incidence of acute radiation pneumonitis (aRPs) in in patients with prior receipt of immune checkpoint inhibitors. 2. Risk factors (especially analysis of the dosimetric risk factor) which may affect the product of aRPs events. 3. Establish a model to predict aRPs and guide clinical treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05219851
Study type Observational
Source Hubei Cancer Hospital
Contact Guang Han, MD.;Ph.D
Phone 13886048178
Email hg7913@hotmail.com
Status Recruiting
Phase
Start date June 1, 2022
Completion date October 31, 2025

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