Collecting data on proton therapy for cancer treatment
Official title: Advanced Proton Therapy Approaches: a Multicenter High-quality Data Registry
Run by European Institute of Oncology · NCT05860361 · Data updated 2026-11-12
This study is collecting information on how well proton therapy works for cancer treatment to help improve care for patients.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 2000 (estimated) |
| Sponsor | European Institute of Oncology Academic / other |
| Locations | 1 site (Milan) |
| Status | Recruiting |
| Started | April 14, 2023 |
| Main results expected | October 1, 2028 |
| Study ends | October 1, 2030 |
| Registry record updated | June 18, 2024 |
| Trial ID | NCT05860361 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients with any type of oncological disease who are eligible for proton therapy.
✕Probably not a fit
Patients under 18 years of age will not benefit from this study as they are excluded from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This registry aims to prospectively gather high-quality data on patients undergoing proton therapy for various oncological conditions. It focuses on understanding the feasibility and clinical outcomes of hypofractionated treatment schedules. The study will implement a three-level data collection approach, including clinical outcomes, radiological analysis, and biological research. By addressing the current lack of robust evidence in proton therapy, this registry seeks to enhance knowledge and improve treatment protocols.
Why it matters
Potential benefit: If successful, this registry could lead to improved treatment strategies and outcomes for cancer patients receiving proton therapy.
How similar studies have gone: While there is limited data on proton therapy, similar registries have shown promise in enhancing treatment understanding and outcomes.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion criteria: * diagnosis of oncological disease (benign and malignant disease); * candidates to proton therapy; * able to provide informed consent. Exclusion criteria: \- age \< 18 years.
Where it's running
-
European Institute of Oncology
Milan, Italy Recruiting
Study contacts
- Principal investigator: Roberto Orecchia — European Institute of Oncology
- Study coordinator: Roberto Orecchia, Prof
- Email: roberto.orecchia@ieo.it
- Phone: +39 0257489578
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Understanding what patients want from NSCLC treatment monitoring
Researchers are testing how patients with non-small cell lung cancer feel about and prefer monitoring their symptoms during treatment, with input from patients, caregivers, and clinicians.
-
Single-Port Robotic Lobectomy for Early-Stage NSCLC
This study tests the safety and outcomes of using the da Vinci Single-Port system for lobectomy and lymph node dissection in people with early-stage non-small cell lung cancer.
-
Disparities in Mental Health Screening and Support for Cancer Patients and Families
This study tests whether cancer patients and their families across Europe have equal access to mental health screening and support services.
-
Melanoma Brain Metastases Treated with Stereotactic Radiosurgery and Systemic Therapy
This study looks at how stereotactic radiosurgery for melanoma brain metastases works when patients are also receiving immunotherapy or targeted therapy.
-
Predictive biomarkers for immunotherapy in endometrial cancer
This study tests molecular and epigenetic features to see if they can predict which endometrial cancer patients will respond to immune checkpoint inhibitors.
-
See if Italian patients with cancer experience MRI anxiety and how a translated questionnaire works
This study tests whether an Italian version of an MRI anxiety questionnaire reliably measures anxiety in adults with cancer undergoing whole-body MRI.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.