Evaluating radiation treatment outcomes for uterine cancer
Official title: Evaluation of Toxicity and Outcomes of Different Therapeutic Strategies in Patients With Uterine Neoplasms Treated With Radiotherapy at the Sant'Orsola Polyclinic in Bologna.
Run by IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06774482 · Data updated 2026-11-12
This study looks at how different radiation treatments for uterine cancer affect patients and their side effects to help make treatments better in the future.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 3000 (estimated) |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna Academic / other |
| Drugs / interventions | radiation |
| Locations | 1 site (Bologna) |
| Status | Recruiting |
| Started | May 19, 2021 |
| Main results expected | December 31, 2030 |
| Study ends | December 31, 2030 |
| Registry record updated | January 14, 2025 |
| Trial ID | NCT06774482 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include female patients aged 18 and older with a new or previous diagnosis of malignant uterine neoplasm treated at the Sant'Orsola Polyclinic.
✕Probably not a fit
Patients who choose not to undergo radiation treatment at the Radiotherapy Unit will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study collects data on the radiation treatment of uterine neoplasms, including endometrial and cervical cancers. It aims to evaluate tumor response and potential toxicity associated with different dosages, fractionation, and techniques used in radiotherapy. By analyzing a large sample of patients treated since 2000, the study seeks to identify correlations between treatment characteristics and radiation-induced toxicities, ultimately aiming to personalize treatment and improve patient outcomes.
Why it matters
Potential benefit: If successful, this study could lead to better prediction and prevention of radiation-induced toxicities in patients with uterine neoplasms.
How similar studies have gone: While this approach is systematic, similar studies have shown success in evaluating treatment outcomes and toxicities in cancer therapies.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female patients, aged ≥ 18 years, with a new or previous diagnosis of malignant uterine neoplasm, starting from 01/01/2000, treated at the Radiotherapy Unit of the Sant'Orsola Polyclinic * Obtaining informed consent Exclusion Criteria: * Patients with a new or previous diagnosis of malignant uterine neoplasm who choose not to undergo radiation treatment at the Radiotherapy Unit of the Sant'Orsola Polyclinic
Where it's running
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IRCCS Azienda Ospedaliero - Universitaria di Bologna
Bologna, Italy Recruiting
Study contacts
- Principal investigator: Alessio Giuseppe Morganti, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Study coordinator: Alessio Giuseppe Morganti, MD
- Email: alessio.morganti2@unibo.it
- Phone: +39 0516363136
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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.