Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04986293

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Medical Center Groningen

Groningen, Provincie Groningen, Netherlands, 9700 RB

Actively Recruiting

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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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CPAP or BiPAP for Motion Mitigation During Radiotherapy | DecenTrialz