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Study identifier: NCT07669493 Synced from ClinicalTrials.gov · July 28, 2026
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Cardiac Safety Management and Immune Microenvironment Changes After Thoracic Radiotherapy: A Prospective Observational Study

Condition: MACE, Arrhythmia, Pericardial Effusion and Survival  ·  Sponsor: Hebei Medical University Fourth Hospital

PhaseN/A
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this observational study is to learn about cardiac safety monitoring after thoracic radiotherapy in adults with thoracic tumors. The main question it aims to answer is: Dose dynamic monitoring of cardiac biomarkers, electrocardiography, echocardiography, peripheral blood immune cell subsets, cytokines, chemokines, lipid profiles, and lipid metabolism markers help identify early clinical or subclinical cardiac changes after thoracic radiotherapy? Are cardiac substructure radiation dose parameters associated with early cardiac safety outcomes? Participants receiving thoracic radiotherapy as part of their regular medical care will complete cardiac safety assessments at the end of radiotherapy, 1 month after radiotherapy, and 3 months after radiotherapy.

This description comes directly from the study's public registry record.

Talk to the study team

Yajing Wu, MD  ·  +8618531118178  ·  wjzs19881212@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

The Fourth Hospital of Hebei Medical UniversityShijiazhuang, Hebei, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07669493