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Spots Global Cancer Trial Database for Oral Aromatase Inhibitors Modify the Gut Microbiome

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Oral Aromatase Inhibitors Modify the Gut Microbiome

Official Title: Oral Aromatase Inhibitors Modify the Gut Microbiome Effecting Estrogen Bioavailability

Study ID: NCT05030038

Conditions

Breast Cancer

Study Description

Brief Summary: The purpose of this research is to study the bacteria in participants' gut before receiving a medicine called an aromatase inhibitor for breast cancer and after participants receive medicine for breast cancer.

Detailed Description: Primary Objective: To describe the microbiome shift of gut microbiome from baseline after 4-weeks and 12-weeks of oral aromatase inhibitor treatment. Secondary Objective * To correlate gut microbiome populations with circulating sex hormone metabolite concentrations at baseline and 12 weeks. * To describe the correlation of change in the microbiome populations with change in circulating sex hormone metabolite concentrations from baseline to 12 weeks.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Wake Forest Baptist Health Sciences, Winston-Salem, North Carolina, United States

Contact Details

Name: Katherine Ansley, MD

Affiliation: Wake Forest Baptist Health Sciences

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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