Actively Recruiting

Age: 16Years - 105Years
All Genders
ID05192876

Analysis of Outcomes and Adverse Events of Patients Undergoing Radiation Therapy Using Patient Records from 2000 to 2025

Led by Daniel Zwahlen · Updated on 2025-05-21

25000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are analyzing the outcomes and side effects experienced by patients undergoing radiation therapy. This observational study uses a database of patient records from the year 2000 to 2025 to systematically record and evaluate treatment results and adverse events. The goal is to improve the quality of radiotherapy and reduce serious side effects for future patients through detailed data analysis and quality control. The study collects data from patients treated with radiotherapy at the Department of Radiation Oncology at the Winterthur Cantonal Hospital. It focuses on tracking overall survival and progression-free survival over 25 years, while also identifying risk factors that influence treatment outcomes. The study also monitors both acute and late adverse events related to radiation therapy. Participants' personal and treatment-related data are systematically recorded and analyzed to assess the effectiveness and safety of radiotherapy. The study evaluates outcomes such as survival rates and side effects to inform future improvements in care. This long-term data collection and analysis supports quality assurance and contributes to clinical research at the Institute for Radio-Oncology.

CONDITIONS

Brief Title

Analysis of Outcomes and Adverse Events of Patients Undergoing Radiation Therapy

Who Can Participate

Age: 16Years - 105Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who are being treated with radiotherapy at the Department of Radiation Oncology at the Winterthur Cantonal Hospital
Not Eligible

You will not qualify if you...

  • Patients not treated with radiotherapy at the Department of Radiation Oncology at the Winterthur Cantonal Hospital
  • Age younger than 16 years
  • Age older than 105 years

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - Up to 25 years

Participants who undergo routine radiotherapy are observed to record outcomes and adverse events over time.

Trial Site Locations

Total: 1 location

1

Kantonsspital Winterthur

Winterthur, Canton of Zurich, Switzerland, 8401

Actively Recruiting

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Research Team

D

Daniel R Zwahlen, MD, MBA

R

Romy Frey

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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https://pubmed.ncbi.nlm.nih.gov/38310268