Actively Recruiting
Proton Therapy Medical Registry for Cancer Patients
Led by Clinica Universidad de Navarra, Universidad de Navarra · Updated on 2021-12-09
6000
Participants Needed
2
Research Sites
1043 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are establishing a registry at the Clinica Universidad de Navarra Proton Therapy Unit to collect detailed information on cancer patients receiving proton radiation therapy. The study aims to capture radiation dosimetry data, baseline clinical information, and track disease progression, toxicities, and quality of life outcomes. This effort seeks to support future analyses to understand which patients may benefit most from proton therapy in a personalized medicine context. The study involves enrolling all patients treated at the proton therapy center, where data on their radiation treatments and clinical outcomes are recorded in the registry. There is no comparison group since this is an observational study documenting real-world treatment experiences with proton radiation. Participants' involvement includes providing clinical data over a long-term follow-up period of up to 20 years. Researchers will monitor treatment effects, toxicities, and quality of life through ongoing data collection without additional interventions. This registry aims to gather comprehensive outcomes to inform future research on proton therapy benefits and risks.
CONDITIONS
Brief Title
Proton Therapy Medical Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients treated at the proton center
You will not qualify if you...
- Any other than what is supplied in the inclusion criteria
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 20 years
Participants who undergo routine care with proton radiation therapy are observed to evaluate disease and toxicity outcomes over an extended period.
Trial Site Locations
Total: 2 locations
1
Clinica Universidad de Navarra
Pamplona, Navarre, Spain, 31008
Actively Recruiting
2
Clinica Universidad de Navarra
Madrid, Spain, 28027
Actively Recruiting
Research Team
F
Felipe A Calvo
U
UCEC UCEC
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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