Rectal Cancer Clinical Trial
Official title:
MRI T1 Relaxation Times in Evaluating Neoadjuvant Treatment of Rectal Cancer
The goal of this observational study is to learn about the T1 relaxation time and T1 relaxation time properties of the disease in people with locally advanced rectal cancer. The main question it aims to answer is: Does MRI T1 relaxation time have a high diagnostic performance in recognizing fibrosis as a complete response to neoadjuvant treatment of rectal cancer? Participants will receive standard neoadjuvant treatment and be part of the standard examination programme regarding rectal cancer.
Status | Recruiting |
Enrollment | 108 |
Est. completion date | December 31, 2025 |
Est. primary completion date | July 30, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - rectal cancer, age >18 years Exclusion Criteria: - contraindications for MRI (pacemaker, claustrophobia, implanted medical injectors and nerve stimulators), - previous radiochemotherapy or another disease which investigator judges inappropriate for the persons continued participation. |
Country | Name | City | State |
---|---|---|---|
Denmark | Vejle Hospital | Vejle | Jylland |
Lead Sponsor | Collaborator |
---|---|
Vejle Hospital |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Difference in T1 relaxation time (ms) in the rectal cancer tumor measured in IntelliSpace-software before and after neoadjuvant radiochemotherapy. | An MRI T1 relaxation time-map is performed on each participant. The data is transferred to IntelliSpace-software for measurement and mapping. It is measured in miliseconds (ms) before and after neoadjuvant treatment. | 6 to 8 weeks. |
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