Colonic Neoplasms Clinical Trial
Official title:
Evaluation of Computed Tomography and Magnetic Diffusion Resonance Imaging in the Preoperative Staging of Colon Cancer
NCT number | NCT05727007 |
Other study ID # | CTMR |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 23, 2019 |
Est. completion date | May 15, 2023 |
Verified date | October 2023 |
Source | Larissa University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this study is the evaluation of different imaging methods for the optimal preoperative staging of colon cancer patients. Imaging findings will be compared with the histopathologic results of the specimen following surgical resection.
Status | Completed |
Enrollment | 120 |
Est. completion date | May 15, 2023 |
Est. primary completion date | March 15, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility | Inclusion Criteria: - Histologically confirmed colonic adenocarcinoma - Patient 18 to 90 years old - Abscence of comorbidities that may affect treatment - Signed informed consent of the patient Exclusion Criteria: - Inability to receive or contraindication for intravenous contrast - Renal impairment - Previous allergies to intravenous contrasts - Incompatible implants with magnetic resonance imaging - Claustrophobia - Active sepsis or systemic infection - Untreated physical and mental disability - Lack of compliance with the protocol process - Non-granting of signed informed consent |
Country | Name | City | State |
---|---|---|---|
Greece | Department of Surgery, University Hospital of Larissa | Larissa |
Lead Sponsor | Collaborator |
---|---|
Larissa University Hospital | University of Thessaly |
Greece,
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Diagnostic accuracy in T stage | Evaluation of diagnostic accuracy in the T stage assessment. Diagnostic accuracy will be evaluated in terms of specificity (true negative rate) | 1 month postoperatively | |
Secondary | Diagnostic accuracy in N stage | Evaluation of diagnostic accuracy in the presence of local or distant metastatic lymph nodes. Diagnostic accuracy will be evaluated in terms of specificity (true negative rate) | 1 month postoperatively | |
Secondary | Diagnostic accuracy in the retroperitoneal resection margin | Evaluation of diagnostic accuracy in the retroperitoneal resection margin. Diagnostic accuracy will be evaluated in terms of specificity (true negative rate) | 1 month postoperatively | |
Secondary | Diagnostic accuracy in peritoneal or nearby organ infiltration | Evaluation of diagnostic accuracy in the peritoneal or nearby organ infiltration. Diagnostic accuracy will be evaluated in terms of specificity (true negative rate) | 1 month postoperatively |
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