Length of Tumour Feeding Artery After Colon Cancer Surgery (ColonCT)
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|ClinicalTrials.gov Identifier: NCT02164149|
Recruitment Status : Unknown
Verified June 2014 by University of Aarhus.
Recruitment status was: Recruiting
First Posted : June 16, 2014
Last Update Posted : June 16, 2014
The quality of colon cancer surgery is highly debated these years since the mortality of the disease is not declining markedly. Surgery is the main treatment of colon cancer and during surgery it is very important for the surgeon to remove the tumour and all potential ways of tumour spread. As colon cancer first of all spreads to the nearby lymph nodes lying along the tumour feeding artery the surgeon aims to cut the vessel as central as possible. This means that all of the tumour feeding artery should have been removed after surgery.
In this study the investigators want to measure the length of the tumour feeding artery after surgery as a quality control of the surgery. The investigators hypothesize that the artery will be shorter than 5 mm.
The investigators wish to CT scan all patients two days after colon cancer surgery and afterwards measure then length of the artery on the images. This study will not inflict with the normal routine for patient information and treatment.
|Condition or disease||Intervention/treatment|
|Colon Cancer||Other: Patients with primary colon cancer|
|Study Type :||Observational|
|Estimated Enrollment :||65 participants|
|Official Title:||Length of Tumour Feeding Artery After Colon Cancer Surgery|
|Study Start Date :||May 2014|
|Estimated Primary Completion Date :||November 2014|
|Estimated Study Completion Date :||November 2015|
Quality of colon cancer surgery
Patients with primary colon cancer
Other: Patients with primary colon cancer
CT scan two days after surgery
- CT scan after colon cancer surgery. The length of the tumour feeding artery will be measured on the images. [ Time Frame: 6 to 9 months ]Patients will have an extra CT scan two days after surgery.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02164149
|Contact: Ditte Munkedal, MD||+45 7846 7710||Ditte.Munkedal@viborg.rm.dk|
|Contact: Soren Laurberg, Professor||+45 7846 email@example.com|
|Aarhus University Hospital||Recruiting|
|Aarhus, Denmark, 8000|
|Contact: Ditte Munkedal, MD +45 7846 7710 Ditte.Munkedal@viborg.rm.dk|
|Study Director:||Soren Laurberg, Professor||Aarhus University Hospital|