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Abdominal compression device to limit breathing motion during lung cancer radiotherapy

Tests whether a compression device reduces breathing movement in adults with lung cancer.

Key facts

Who runs it
Tianjin Medical University Cancer Institute and Hospital
Where
Tianjin, ChinaSee the site
Trial code
Registry title
Feasibility and Effectiveness of Respiratory Movement Management in Lung Cancer Receiving Stereotactic Radiotherapy Using a Novel Positional Fixation Device
Status
Recruiting
People taking part
50 people, planned
Started
10 May 2026
Expected to end
31 Dec 2026
Type of study
Observational, 2 groups
Treatments tested
  • Chest and abdominal compression
  • breathing management
Record updated
1 May 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with a single lung cancer tumor at the edge of the lung who can have stereotactic body radiotherapy (SBRT). It tests a belly pressure device that limits breathing movement.

Age
18 years or older
Sex
All sexes can join
Disease stage
One solitary peripheral lung cancer, judged by the doctors to be treatable with SBRT

Main reasons for not taking part

  • Central or super central lung cancer in people who cannot or do not want to have breathing suppression and chest and abdominal compression fixation

The registry criteria, word for word

Show all 2 criteriaShow less

Who can take part

  • 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

Who cannot take part

  • Central or super central lung cancer patients who are intolerant or unwilling to undergo respiratory suppression and chest and abdominal compression fixation

Where in China

  • Tianjin Medical University Cancer Institute and HospitalTianjin, ChinaContact: Xu Yao YuTaking people

About the trial

What the trial wants to find out

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:

Read full original descriptionShow less

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

The 2 groups in the trial

  • Breathing management group

    CT/4DCT scan under breathing management

    Treatment: Chest and abdominal compression and breathing management

  • No breathing management group

    CT/4DCT scan under free breathing

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
A Single Center, Translational Study on the Feasibility and Effectiveness of Respiratory Movement Management in Lung Cancer Patients Receiving Stereotactic Radiotherapy Using a Novel Positional Fixation Device
Plain-language title
Abdominal compression device to limit breathing motion during lung cancer radiotherapyGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 13 November 2026.
Record updated
1 May 2026