Actively Recruiting
Advances in Imaging to Assess Response in Rectal Cancer
Led by NHS Greater Glasgow and Clyde · Updated on 2025-02-12
20
Participants Needed
1
Research Sites
84 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational study is to determine the feasibility of acquiring serial MRI images for advanced radiotherapy planning in colorectal patients. The main question it aims to answer: Is it feasible to acquire serial MR images for advanced radiotherapy planning for rectal cancer.
CONDITIONS
Official Title
Advances in Imaging to Assess Response in Rectal Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Histologically confirmed rectal adenocarcinoma.
- T stage 3b or above and/or high risk factors such as EMVI or nodal disease.
- Participant able to give written informed consent.
- Male or non-pregnant female 18 years of age or older.
- Scheduled to undergo radical radiotherapy.
- Patients willing and able to comply with the protocol for the duration of the study.
You will not qualify if you...
- Contraindications to MRI including claustrophobia, excessive body weight, MRI unsafe implants, ferrous metal in the body, or insufficient information on prior surgeries.
- MRI conditional implants where conditions cannot be met, such as pacemakers.
- Any previous radiotherapy to the pelvis.
- Inflammatory bowel disease.
- Other severe or uncontrolled systemic diseases or significant disorders that make participation undesirable, as determined by the treating clinician.
- History of physical or psychiatric disorders that prevent informed consent or protocol compliance.
- Patients with de-functioning stoma.
- Major surgery within 28 days prior to trial entry.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beatson West of Scotland Cancer Centre
Glasgow, United Kingdom, G120YN
Actively Recruiting
Research Team
M
Ms Lynsey Devlin
CONTACT
M
Ms Aileen Duffton, PhD Cancer Sciences
CONTACT
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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