Radiotherapy Treatments for Neoplasms in the Abdominal-pelvic Region
1 other identifier
observational
7,700
1 country
1
Brief Summary
Evaluation of clinical and dosimetric aspects, tolerance, and effectiveness of abdominal-pelvic region radiotherapy treatments in patients undergoing radiotherapy for primary or secondary neoplasms localized in the abdominal-pelvic region.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2018
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 22, 2018
CompletedFirst Submitted
Initial submission to the registry
March 22, 2024
CompletedFirst Posted
Study publicly available on registry
March 28, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedAugust 5, 2024
March 1, 2024
6.9 years
March 22, 2024
August 2, 2024
Conditions
Outcome Measures
Primary Outcomes (2)
Overall survival
Number of patients death
5 years
Disease free survival
Number of oncological event (local recurrence, distant metastasis, other primary tumor)
5 years
Study Arms (1)
Radiotherapy to abdominal-pelvic region
Collection of data of patients receiving RadioTherapy (RT) to abdominal-pelvic region
Eligibility Criteria
Patients treated at European Institute of Oncology with radiotherapy for curative, palliative, neo-adjuvant, and adjuvant purposes in the abdominal-pelvic region
You may qualify if:
- Patients treated with radiotherapy for curative, palliative, neo-adjuvant, and adjuvant purposes in the abdominal-pelvic region for:
- Primary tumors of the gastrointestinal tract, Primary tumors of the male and female reproductive systems, Primary tumors of the urinary system, Primary tumors of the cardio-circulatory system, Primary tumors of the lymphatic system, Primary tumors of the nervous system, Skin tumors, Secondary abdominal-pelvic localizations of various origins, Primary or secondary bone or soft tissue lesions of the lumbosacral spine and pelvis.
- Signed informed consent
You may not qualify if:
- \. Radiotherapy in districts other than the abdominal-pelvic region
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
European Institute of Oncology
Milan, Italy
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Barbara Alicja Jereczek
European Institute of Oncology
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 22, 2024
First Posted
March 28, 2024
Study Start
February 22, 2018
Primary Completion
December 31, 2024
Study Completion
December 31, 2024
Last Updated
August 5, 2024
Record last verified: 2024-03