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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00280332
Other study ID # FUC
Secondary ID
Status Completed
Phase N/A
First received January 20, 2006
Last updated May 9, 2008
Start date March 2006
Est. completion date November 2007

Study information

Verified date May 2008
Source Chinese University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority Hong Kong: Department of Health
Study type Observational

Clinical Trial 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


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.


Recruitment information / eligibility

Status Completed
Enrollment 560
Est. completion date November 2007
Est. primary completion date November 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 50 Years to 75 Years
Eligibility Inclusion Criteria:

- Subjects who are previously participated in one of our two screening colonoscopy studies [Sung, Gastroenterol 2003; Leung, AJG 2004]

- Asymptomatic on first screening colonoscopy

- Age>50and <75

- No family history of CRC

- No other colonoscopy except the baseline screening colonoscopy

Exclusion Criteria:

- Subjects who refused consent

- Subjects who are not warrant follow up colonoscopy

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
colonoscopy
proform a follow up colonoscopy in the 5 year period from index colonoscopy

Locations

Country Name City State
China Endoscopy Center, Prince of Wales Hospital Hong Kong (SAR)

Sponsors (1)

Lead Sponsor Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The prevalence of advanced colonic adenoma in the re-screening population 5 year from index colonoscopy No
Secondary The time to adenoma adenoma development according to different baseline characteristics of patients and colonoscopy findings 5 years from index colonoscopy No
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