UZ Leuven
Leuven, 3000, Belgium
Location status: Recruiting
NCT Number: NCT07373782
This study is a prospective, non-randomized clinical study aimed at investigating the potential benefits of continuous positive airway pressure (CPAP) support during radiotherapy for breast cancer. CPAP is a device commonly used to support breathing, for example in patients with sleep apnea. The investigators expect a reduction in radiation doses to the heart and/or lungs with CPAP-supported radiotherapy compared to standard radiotherapy (without CPAP), which may also lead to a decrease in radiation-induced heart and/or lung conditions in the long term. The study will also examine how the use of a CPAP device can be implemented in daily radiotherapy practice.
Interested in participating?
Request Info40 year–80 year
Female
Interventional
Phase 2 / Phase 3
Leuven, 3000, Belgium
Location status: Recruiting
Patients undergoing breast conserving surgery for invasive or in situ BC and requiring adjuvant RT are prospectively enrolled -either left-sided cases with or without regional nodal irradiation (RNI), or right-sided cases requiring RNI. Each patient undergoes an additional CT simulation with continuous positive airway pressure (CPAP) (15cm H20) -in free breathing (FB) for right-sided cases and in deep inspiration breath hold (DIBH) for left-sided cases. Left-sided patients unable to perform DIBH are evaluated in FB. Two RT plans (with and without CPAP) are dosimetrically compared. If CPAP reduces mean heart or CLB dose by ≥0.5 Gy, or mean lung dose by ≥1 Gy, treatment is delivered with CPAP. Patient comfort is assessed through surveys.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Positive airway pressure (15cmH2O) delivered by a CPAP-device
Time frame: From enrollment to the end of treatment at +/-8 weeks
Potential change of mean radiation dose to the heart
Time frame: From enrollment to the end of treatment at +/-8 weeks
Potential change in radiation dose to cardiac substructures
Time frame: From enrollment to the end of treatment at +/-8 weeks
Potential change in mean radiation dose to the lungs
Time frame: From enrollment to the end of treatment at +/-8 weeks
Potential change in mean radiation dose to the contralateral breast
Time frame: From enrollment to the end of treatment at +/-8 weeks
Potential change in radiation dose to the liver
Time frame: From enrollment to the end of treatment at +/-8 weeks
Patient comfort assessed through patient questionnaires (Likert scale: Strongly disagree - disagree - neutral - agree - strongly agree)
Time frame: From enrollment to the end of treatment at +/-8 weeks
Compare reproducibility and accuracy between standard and CPAP-assisted RT by using surface scanning and daily cone beam CT (CBCT) parameters
Time frame: From enrollment to the end of treatment at +/-8 weeks
To compare DIBH performance between standard and CPAP-assisted RT for left-sided BC by using surface scanning and daily CBCT parameters
Time frame: From enrollment to the end of treatment at +/-8 weeks
To compare time-effectiveness between standard and CPAP-assisted RT
Interested in participating?
Request InfoUniversitaire Ziekenhuizen KU Leuven
Other
Reducing Cardiac Radiation Dose in Continuous Positive Airway Pressure (CPAP) Assisted Radiotherapy in Breast Cancer: a Prospective Non-Randomized Clinical Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07797218
Breast Cancer Early Stage Breast Cancer (Stage 1-3), Breast Diseases
Shanghai, China
View Trial DetailsNCT06970912
Breast Cancer Early Stage Breast Cancer (Stage 1-3), Breast Diseases
Beijing, Beijing Municipality, China
View Trial DetailsNCT06930521
Breast Cancer, Breast Cancer Early Stage Breast Cancer (Stage 1-3)
Toronto, Ontario, Canada
View Trial DetailsNCT07273357
Adjuvant Drug Therapy, Breast Cancer Early Stage Breast Cancer (Stage 1-3)
Gävle, Sweden
View Trial Details