Ignite Creation Date:
2024-05-06 @ 10:23 AM
Last Modification Date:
2024-10-26 @ 12:29 PM
Study NCT ID:
NCT03249727
Status:
TERMINATED
Last Update Posted:
2023-01-31
First Post:
2017-08-10
Brief Title:
Analysis of Natural Killer Cell Activity NKA in Whole Blood in High Risk Subjects Undergoing Colonoscopy
Sponsor:
ATGen Canada Inc
Organization:
ATGen Canada Inc
Study Overview
Official Title:
Analysis of Natural Killer Cell Activity NKA in Whole Blood in High Risk Subjects Undergoing Colonoscopy
Status:
TERMINATED
Status Verified Date:
2023-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Recruiting issues
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
ANKA-HR
Brief Summary:
This study will measure the activity of natural killer NK cells using the in vitro diagnostic device NK Vue in high risk subjects Quebec risk categories P2 P3 and P4 scheduled for colonoscopy
Detailed Description:
In Quebec subjects in risk category P2 are scheduled for colonoscopy due to high suspicion of cancer based on imaging sigmoidoscopy or clinical exam Subjects in categories P3 and P4 are scheduled for colonoscopy for one of the following reasons suspicion of having an inflammatory bowel condition rectal bleeding presence of occult blood in stool unexplained iron deficiency anemia recent change in bowel habits family history of CRC or adenomatous polyps or other hereditary colorectal diseases Often colonoscopy is not performed within the government-prescribed recommended delays leading to waiting lists for the procedure Analysis of NK cell activity may help identify those at risk for the presence of CRC and therefore help prioritize subjects on these waiting lists help manage resources and help convince subjects to have a colonoscopy Furthermore all subjects will undergo a FIT allowing a determination of the ability of each test alone as well as a combination of NK Vue and FIT to predict outcome on colonoscopy
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None