Ignite Creation Date:
2024-05-05 @ 4:38 PM
Last Modification Date:
2024-10-26 @ 9:22 AM
Study NCT ID:
NCT00280332
Status:
COMPLETED
Last Update Posted:
2008-05-12
First Post:
2006-01-20
Brief Title:
A Follow-up Colonoscopy Examination in Patients Who Had Previously Undergone Screening Colonoscopy
Sponsor:
Chinese University of Hong Kong
Organization:
Chinese University of Hong Kong
Study Overview
Official Title:
A Follow-up Colonoscopy Examination in Patients Who Had Previously Undergone Screening Colonoscopy
Status:
COMPLETED
Status Verified Date:
2008-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
To determine the prevalence of colonic neoplasm in patients who had previously undergone screening colonoscopy
To determine the optimal time interval for re-screening in average risk individuals
To determine potential baseline characteristics that predicts adenoma recurrence
To determine the optimal time interval for re-screening in average risk individuals
To determine potential baseline characteristics that predicts adenoma recurrence
Detailed Description:
Colorectal cancer CRC is the second commonest cancer in Hong Kong and tends to be increasing Screening for colorectal cancer can reduce the cancer incidence and mortality by detecting early lesions However the best interval for a follow up colonoscopy particularly for those with normal baseline colonoscopy remains largely unknown
This study aim to determine the prevalence of colonic neoplasm in average-risk patients who had previously undergone screening colonoscopy and the optimal time interval for re-screening
This study aim to determine the prevalence of colonic neoplasm in average-risk patients who had previously undergone screening colonoscopy and the optimal time interval for re-screening
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None