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Clinical Trial Summary

The primary objective of the study is to determine whether there is a correlation between the intestinal side effects of chemotherapy treatment and the expression/activity profiles of glucuronidase enzymes in the stool microbiome of the target patient population.


Clinical Trial Description

STUDY DESIGN: - This protocol is a single-center, single-cohort, bioresearch study enrolling up to 8 participants. The cohort is as follows: - Cohort 1: Colorectal Cancer: (n=8) - The study will enroll participants per the eligibility criteria. - Participants will have 2 scheduled at-home stool self-collections at the time points specified in section 4.0 and complete a questionnaire by telephone contact (see section 11.0 for details). The biospecimens collected from participants on this study are stool samples. - Confirmation of eligibility and medical record review by a member of the study staff will be completed for participants of the disease cohort before they are considered fully enrolled. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05821582
Study type Observational
Source Sanguine Biosciences
Contact
Status Withdrawn
Phase
Start date March 27, 2023
Completion date October 5, 2023

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