Actively Recruiting
CPAP or BiPAP for Motion Mitigation During Radiotherapy
Led by University Medical Center Groningen · Updated on 2026-05-04
31
Participants Needed
1
Research Sites
339 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
When using highly conformal radiotherapy techniques, such as proton therapy, a controlled breathing pattern and a minimal breathing amplitude could greatly benefit the treatment of mobile tumors. This reduction in tumor motion may be achieved with the use of a ventilator that is able to regulate and modulate the breathing pattern. CPAP provides a constant level of positive airway pressure. Compared to spontaneous breathing, the use of CPAP increased lung volume and can result in a significant decrease in tumor movement and a significant decrease in both mean lung and mean heart radiation dose. These results were found in patients treated for limited stage disease, it is not clear if this approach is feasible for patients with more advanced stage of disease that undergo radiotherapy with curative intent. With Bilevel Positive Airway Pressure (BiPAP), tidal volume excursions are determined by the pressure difference between the set inspiratory positive airway pressure (IPAP) and the set expiratory positive airway pressure (EPAP). This mode of ventilation increases lung volume comparable to CPAP, but also to control tidal volumes and breathing frequency. However, BiPAP has never been studied in the setting of motion mitigation during radiotherapy and BiPAP might be more difficult to adjust to for patients compared to CPAP. Therefore, the current study is proposed to evaluate whether or not CPAP or BiPAP is of benefit in patients that undergo radiotherapy for larger intra-thoracic tumor volumes.
CONDITIONS
Official Title
CPAP or BiPAP for Motion Mitigation During Radiotherapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosed with stage III or IV non-small cell lung cancer, esophageal cancer, or malignant lymphoma planned for curative radiotherapy
- WHO performance status 0 to 2
- Able to provide written informed consent
You will not qualify if you...
- Facial deformities preventing proper fitting of facial mask
- Not meeting any inclusion criteria
- Planned radiotherapy with fraction dose of 3 Gy or higher
- Severe heart failure with left ventricular ejection fraction below 30%
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University Medical Center Groningen
Groningen, Provincie Groningen, Netherlands, 9700 RB
Actively Recruiting
Research Team
R
Robin Wijsman
CONTACT
J
J. Elshof
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
0
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