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NCT00591279 Clinical Trial

Cancer Control Following Polypectomy

Colon Cancer Clinical Trial

Official title:
Cancer Control Following Polypectomy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00591279
Other study ID # 81-035
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1981
Est. completion date January 2017

Study information
Verified date September 2023
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates strategies for the surveillance of post-polypectomy patients for the control of bladder cancer

Recruitment information / eligibility
Status Completed
Enrollment 110
Est. completion date January 2017
Est. primary completion date January 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - referral for colonoscopy or - referral for proctoscopy or for a complete colonoscopy after a proctoscopy or flexible sigmoidoscopy Exclusion Criteria: - prior history of colon cancer, unrelated polypectomy, inflammatory bowel disease, family history of familial polyposis

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Memorial Sloan Kettering Cancer Center New York New York

Sponsors (9)
Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center Cedars-Sinai Medical Center, Massachusetts General Hospital, Medical College of Wisconsin, Minneapolis Veterans Affairs Medical Center, Mount Sinai Hospital, New York, National Cancer Institute (NCI), St. Lukes hospital in Racine, Wiscousin, Valley Presbyterian Hospital

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary evaluate strategies for the surveillance of post-polypectomy patients 6 years
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