Japanese National Computed Tomographic (CT) Colonography Trial
This trial is active, not recruiting.
|Conditions||colonic polyps, colonic neoplasms|
|Treatment||ct colonography and optical colonoscopy|
|Sponsor||Japanese CT Colonography Society|
|Start date||October 2009|
|End date||January 2013|
|Trial size||1500 participants|
|Trial identifier||NCT00997802, JANCT-01, UMIN000002097|
The purpose of this study is to evaluate the sensitivity of computed tomographic colonography (CTC) in detecting colorectal polyps and cancers in 1,500 subjects at increased risk of colorectal cancer (CRC), using optical colonoscopy as the reference standard.
|United States||No locations recruiting|
|Other Countries||No locations recruiting|
|Boston, MA||Japanese CTC Society, 3D imaging Laboratory, Massachusetts General Hospital||no longer recruiting|
|Otaru, Japan||Otarukyokai Hospital||no longer recruiting|
|Sapporo, Japan||Hokkaido Gastroenterology Hospital||no longer recruiting|
|Sapporo, Japan||Hokkaido Social Insurance Hospital||no longer recruiting|
|Sapporo, Japan||Tonan Hospital||no longer recruiting|
|Kanazawa, Japan||Kanazawa University Hospital||no longer recruiting|
|Yokohama, Japan||Showa University Northern Yokohama Hospital||no longer recruiting|
|Kamigoto, Japan||Kamigoto Hospital||no longer recruiting|
|Kurashiki, Japan||Kawasaki Medical School||no longer recruiting|
|Hamamatsu, Japan||Hamamatsu South Hospital||no longer recruiting|
|Shimono, Japan||Jichi Medical University Hospital||no longer recruiting|
|Arakawa-ku, Japan||Tokyo Women's Medical University Medical Center East||no longer recruiting|
|Intervention model||single group assignment|
sensitivity in the detection of colorectal polyps and cancers in CTC
time frame: 1.5 years
specificity and predictive values in the detection of colorectal polyps and cancers in CTC.
time frame: 1.5 years
Male or female participants at least 20 years old.
Inclusion Criteria: - Outpatients who are eligible for optical colonoscopy. - Aged 20 years or older. - Major functions of organs of the subjects are in a good condition. - Signed informed consent forms are obtained from the patients. Exclusion Criteria: - Known colorectal polyps or cancers at any site at the time of enrollment. - Patients with inflammatory bowel disease. - Fulfillment of clinical criteria for diagnosis of FAP or HNPCC (Amsterdam criteria). - Serious medical conditions that may increase the risk of optical colonoscopy or are so severe that screening would have no benefit. - Previous colorectal surgery. - Gastric or intestinal stenosis, abdominal adhesions, bowel obstruction or perforation, toxic megacolon. - Evidence of an increased risk in carrying out bowel preparation or CTC exams. - Possibility of pregnancy. - Optical colonoscopy or barium enema carried out within the last 3 years. - Patients with psychological conditions that contraindicate colonoscopy or that make them irrelevant to participate in the trial. - Iodine hypersensitivity. - Severe thyroid disease. - Claustrophobia. - Severe deafness. - Subjects whose eligibility for this clinical trial is not appropriate by other reasons.
|Official title||Evaluation of Accuracy of Computed Tomographic Colonography (CTC) in the Diagnosis of Colorectal Tumors by Gastroenterologists and Radiologists With Computer-aided Detection (CAD): A Multicenter Study|
|Description||The investigators will evaluate the sensitivity of CTC in detecting colorectal polyps and cancers (at least 6 mm in diameter) in 1,500 subjects at increased risk of colorectal cancer (CRC), using optical colonoscopy as the reference standard. The primary endpoint will be sensitivity in the detection of colorectal polyps and cancers that are at least 6 mm in diameter. The secondary endpoints will include specificity and predictive values in the detection of colorectal polyps and cancers. This clinical study will also evaluate the differences of the detection accuracies between human readings with and without computer-aided detection (CAD) that automatically detects colonic lesions in CTC images and presents the detected lesions to the readers. This clinical study will also compare performance between radiologists and gastroenterologists in detecting colorectal lesions in CTC images. All the CTC images and their interpretations, optical colonoscopy reports and images, and pathology reports of resected colorectal lesion will be prospectively collected from 12 Japanese hospitals participating in the trial. All patients' information will be completely anonymized at each site before any analysis of the data takes place.|
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