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NCT02596516 Clinical Trial

A Comparison of Colonic Bile Acid Content Following Right and Left Colectomies

Colectomy Clinical Trial

Official title:
A Comparison of Colonic Bile Acid Content Following Right and Left Colectomies

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT02596516
Other study ID # MMC-0249-15
Secondary ID
Status Not yet recruiting
Phase N/A
First received November 2, 2015
Last updated November 5, 2015
Start date December 2015
Est. completion date December 2020

Study information
Verified date November 2015
Source Meir Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

The aim of this study is to evaluate whether there is a difference in the bile acid content in the bowel in patients after right versus left colectomy. There is compelling evidence that patients under going resection of the right colon versus left coolon have a lower polyp detection rate in surveillance colonoscopies. The investigators intend to evaluate feces of patients undergoing left and right colectomies; prior to their surgery and again three and six months aftet the surgery. The investigators plan to compare the content of the different bile acids and to compare the content between the two groups.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 100
Est. completion date December 2020
Est. primary completion date January 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age above 18.

- Patients intended to undergo a colectomy for colonic cancer

- Patients willing and participate and able to sign an informed consent

Exclusion Criteria:

- Age under 18.

- Patients with Inflammatory Bowel Disease (Crohn's, Ulcerative colitis).

- Patients refusing to participate or are unable to understand or sign an informed consent

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Meir Medical Center

Outcome
Type Measure Description Time frame Safety issue
Primary Colonic bile acid content two years No
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