Feasibility and Effectiveness of Respiratory Movement Management in Lung Cancer Receiving Stereotactic Radiotherapy Using a Novel Positional Fixation Device
Tianjin Medical University Cancer Institute and Hospital
Phase
Observational
Started
2026-05-10
Last updated
2026-05-01
Condition(s) studied
Lung Cancer, Non-Small Cell
Investigational drug(s) / intervention(s)
Chest and abdominal compressionbreathing management
Chest and abdominal compression: Abdominal compression suppresses respiratory movement in patients
breathing management: Apply pressure to the patient's abdomen to achieve respiratory movement inhibition
Study summary
The purpose of this clinical trial is to understand the safety and effectiveness of abdominal pressure devices in inhibiting respiratory movement in lung cancer patients. The main question it aims to answer is:
Did the abdominal pressure device reduce the respiratory movement of participants with lung cancer tumors?
Participants will:
Record how much they use abdominal pressure devices to suppress lung cancer tumor respiratory movement
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
Clinical diagnosis is solitary peripheral lung cancer, and after comprehensive evaluation by the participating physicians based on the patient's clinical data, it is suitable for receiving SBRT treatment;
Exclusion Criteria:
Central or super central lung cancer patients who are intolerant or unwilling to undergo respiratory suppression and chest and abdominal compression fixation
Primary outcome measure(s)
Tumor displacement range — Within 6 months after enrollment Based on 4DCT for delineating tumor motion range and extracting radiomics features in patients with and without respiratory management
Trial sites (1)
Facility
City
Region
Status
Tianjin Medical University Cancer Institute and Hospital
Tianjin
China
Recruiting
More Tianjin Medical University Cancer Institute and Hospital trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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