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Human Microbiome clinical trials

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NCT ID: NCT05560087 Recruiting - Periodontitis Clinical Trials

Association of PeRiODontal Disease and gUt Microbiome With Coronary artEry Disease (PRODUCE Study)

Start date: September 20, 2022
Phase:
Study type: Observational

The purpose of this study is to explore the relationship between periodontal disease and coronary artery disease through changes in the gut microbiome. In addition, the investigators aim to find possible periodontal pathogens that have association with cardiovascular disease.

NCT ID: NCT05295719 Not yet recruiting - Obesity Clinical Trials

Combining HIIT and n-3 PUFA to Reduce Inflammation and Improve Metabolic Health

HIIT&PUFA
Start date: April 1, 2022
Phase: N/A
Study type: Interventional

The goal of this project is to understand the combined effects of fish oil and exercise in obesity-associated inflammation. The investigators hypothesize that fish oil will improve gut bacteria profiles, which will in turn potentiate the benefits of an exercise program and improve energy utilization and reduce inflammation and metabolic risk.

NCT ID: NCT05150184 Completed - Human Microbiome Clinical Trials

Isolation and Characterization of Multiple Microbial Species From Diverse Healthy Adults

IsoMic
Start date: November 17, 2021
Phase:
Study type: Observational

Isolation and characterization of fecal/oral/skin/nasal/throat microbial species from a diverse cohort of healthy adults.

NCT ID: NCT04841694 Not yet recruiting - Human Microbiome Clinical Trials

Oral Probiotics on the Shift in Gut Microbiome and Skin Carotenoid Levels

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine how probiotics affects circulating carotenoid levels.

NCT ID: NCT04597502 Completed - Human Microbiome Clinical Trials

The Effects of Terminalia Chebula Fruit Extract on the Gut Microbiome and Skin Biophysical Properties

Start date: October 15, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the use of oral Terminalia chebula fruit extract on the gut microbiome and skin biophysical properties. The fruit is commonly used for skin treatments in India. It is thought to have antioxidant properties, reduce inflammation and affect the microorganisms in the gut. The information the investigators will learn from this study may indicate how and if oral dosing can affect the skin and gut microbiome. This may lead to an improved understanding of the skin and determine whether these oral products are effective for improving the skin's appearance.

NCT ID: NCT04596722 Completed - Human Microbiome Clinical Trials

Oral Pomegranate Extract on the Microbiome and Skin Biophysical Properties

Start date: November 9, 2020
Phase: N/A
Study type: Interventional

Pomegranate extract (Pomella) is well known for its antioxidant properties due to its phenolic compounds. It has also been shown to increase the amount of short chain fatty acid producing Lactobacillus and Bifidobacteria genera. Short chain fatty acids are thought to have an anti-inflammatory effect on the sebaceous glands. Previous studies have concluded that pomegranate extract may act as a prebiotic in the body and subsequently increasing the gastrointestinal microbial diversity and by producing short chain fatty acids that may have systemic beneficial effects especially on the skin. Therefore, the aim of this study is to assess how Pomella alters the gut microbiome and the blood level of short chain fatty acids in healthy subjects.

NCT ID: NCT04335526 Completed - Human Microbiome Clinical Trials

A Clinical Study to Assess the Effect of Change of Bile Acid on the PD and Safety of Metformin and Microbiome Profiles

Start date: May 1, 2020
Phase: Phase 1
Study type: Interventional

This clinical trial is intended to evaluate the effect of change of bile acid pool with cholestyramine on the pharmacodynamics and safety of metformin and intestinal microbiome profiles in healthy volunteers

NCT ID: NCT04222699 Completed - Human Microbiome Clinical Trials

Cultures Before and After Decolonization in Community Dwelling Adults With Current S. Aureus Colonization

Start date: September 18, 2012
Phase: Phase 4
Study type: Interventional

The investigators propose to study the microbiome of the nose, throat and three skin sites in a population without current exposure to the healthcare environment: 80 community dwelling adults. We will characterize the microbial communities in these body sites (nose, throat, perirectal and three skin sites) over time using culture-independent techniques. The investigators will then "decolonize" the subjects. Subjects will receive intranasal mupirocin and topical chlorhexidine. The investigators will then compare the microbial communities at baseline and after decolonization within individuals. Our overall hypothesis is that the microbial composition of these sites and the response to decolonization is influenced by the healthcare environment and that decolonization leads to re-colonization with an increasing proportion of Gram-negative bacilli.

NCT ID: NCT04218799 Completed - Human Microbiome Clinical Trials

Human Microbiome and Healthcare Associated Infections - Nursing Home Dwelling Older Veterans

Start date: August 12, 2014
Phase: Phase 4
Study type: Interventional

The purpose of the research is to find out the effect of commonly used topical antibiotics on the bacteria that live in the nose, throat and on the skin of older adults. In addition, the investigators want to determine if these topical antibiotics affect how bacteria are spread in Community Living Centers of the VA Maryland Health Care System.

NCT ID: NCT03942159 Recruiting - Human Microbiome Clinical Trials

Modification of the Human Colon and Oral Microbiome by Allogenic HSCT

Start date: May 14, 2019
Phase:
Study type: Observational

Allogenic HSCT brings significant changes in biodiversity and composition of the gut microbiome through antibiotic usage, the mucosal damage due to the chemo- and radiotherapy toxicity; compromised oral nutritional intake and graft-versus-host disease with gut damage as the complication. Aim of the study is to investigate the composition of the microbiota in both recipient and nursing relative donor, reveal changes in biodiversity after HSCT via 3-time points V3V4 16S rRNA and NGS sequencing of the colon and oral swabs, 3-indoxyl-sulfate measurement in the urine.