Clinical trial · Interventional
CPAP or BiPAP for Motion Mitigation During Radiotherapy
Continuous and Bi-level Positive Airway Pressure for Motion Mitigation of Intra-thoracic Tumors Treated With Radiotherapy
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Esophageal Cancer | Malignant Esophageal Neoplasm | CURATED_EXACT | 0.92 |
| Malignant Lymphoma | Lymphoma | ALIAS | 0.90 |
| NSCLC | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
| Radiotherapy Side Effect | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CPAP | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Lung volume changes induced by the use of mechanical ventilation
- timeFrame
- 2-3 hours of measurement (only once)
- description
- The primary objective is to evaluate the lung volume changes (in cm3) induced by the use of mechanical ventilation
Secondary outcomes (2)
- measure
- Feasibility of mechanical ventilation
- timeFrame
- once every week up to a maximum of 5 consecutive weeks (depending on the duration of the course of radiotherapy)
- description
- Feasibility is expressed as a score (using a Visual Analoge Scale)
- measure
- Feasibility of mechanical ventilation
- timeFrame
- once every week up to a maximum of 5 consecutive weeks (depending on the duration of the course of radiotherapy)
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Age ≥18 years * Stage III/IV (N)SCLC, esophageal cancer or malignant lymphoma that will be treated with curative intent * WHO 0-2. * Written informed consent Exclusion Criteria: * Facial deformations so that facial mask is impossible to fit * Noncompliance with any of the inclusion criteria. * Planned for radiotherapy with fraction dose ≥3 Gy. * Severe heart failure (LVEF\<30%)
References
Publications (0)
Data not yet available