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Dysbiosis clinical trials

View clinical trials related to Dysbiosis.

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NCT ID: NCT05632497 Recruiting - Anorexia Nervosa Clinical Trials

Alteration of Symbiosis Intestinal Microbiota on Patients With Anorexia Nervosa

INT-METAVOSA
Start date: May 23, 2024
Phase:
Study type: Observational

The purpose of this study will be to study the association between the level of psychic symptomatic of anorexia nervosa (AN) (intensity of food restriction, symptoms of anxiety and depression) and alteration of host environment symbiosis and the mechanism (dysbiosis of intestinal microbiota, increase of intestinal permeability, immunity alteration and low-grade inflammation).

NCT ID: NCT05622721 Recruiting - Clinical trials for Clostridium Difficile

REMBRANDT: REcovery of the MicroBiome fRom Antibiotics for Dental implanTs

Start date: May 30, 2022
Phase:
Study type: Observational

Antimicrobial therapy can lead to disruption of the gut microbiome and infection with Clostridioides difficile, a disease associated with high morbidity and mortality, particularly among the elderly. Drawing on observations that pet ownership and close contact with pets are protective against colonization with C. difficile and recurrence of C. difficile infection, the proposed study will test the hypothesis that microbiota that provide colonization resistance against C. difficile are shared between patients and their pets and that pet contact can mitigate antimicrobial-associated gut dysbiosis and the risk of C. difficile infection. This study will further define epidemiologic and pathophysiologic characteristics of C. difficile infection and gut microbiome dysbiosis that could enhance therapeutic options for these conditions, potentially through non-invasive interventions involving animal contact.

NCT ID: NCT05619055 Recruiting - Clinical trials for Necrotizing Enterocolitis of Newborn

The Intestinal Dysbacteriosis in the Pathogenesis of Necrotizing Enterocolitis

Start date: November 5, 2022
Phase:
Study type: Observational

Study Description The goal of this observational study is to detect intestinal flora and the metabolic products in premature infants diagnosed as necrotizing enterocolitis. The main questions it aims to answer are: - 1. Whether there is intestinal flora in the stool of premature infants. - 2. Are there dysregulated intestinal flora and their metabolic products in premature infants diagnosed as necrotizing enterocolitis. - 3. The detailed role and underlying mechanism of the intestinal dysbacteriosis and the metabolic products in premature infants diagnosed as necrotizing enterocolitis. Participants, premature infants diagnosed as necrotizing enterocolitis (NEC group), will be asked to collect stool (usually 2 times) for intestinal flora analysis. If there is a comparison group: Researchers will compare premature infants without necrotizing enterocolitis (control group) to see if their intestinal flora and the metabolic products also changed as their NEC counterparts.

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: NCT05517928 Recruiting - Healthy Clinical Trials

A Study to Evaluate the Impact of Lactobacillus Rhamnosus GG on Proton Pump Inhibitor-Induced Gut Dysbiosis

Start date: March 3, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the impact of the probiotic Lactobacillus rhamnosus (LGG) on proton pump inhibitor (PPI)-induced changes to the microbes that live in the gastrointestinal tract and are passed out in the stool. PPI medicines reduce stomach acid and are commonly used to treat acid reflux disease.

NCT ID: NCT05407090 Recruiting - Clinical trials for Bariatric Surgery Candidate

The Effect of Probiotics on Systemic Inflammation and Metabolic Endotoxemia in Patients Undergoing Bariatric Surgery

Start date: August 2, 2021
Phase: N/A
Study type: Interventional

This study explores the effects of probiotic administration on the outcomes of surgical treatment, and also on the state of the intestinal microbiota and the intestinal barrier. The study protocol is designed as a randomized double-blind placebo-controlled clinical trial. Patients qualified for bariatric surgery will be randomized to receive probiotics or a placebo for 12 weeks. Researchers are going to evaluate changes in intestinal microbiota, epithelial permeability, weight loss, postoperative complications, and serum parameters reflecting inflammation, metabolic profile, and metabolic endotoxemia.

NCT ID: NCT05288790 Recruiting - HIV Infections Clinical Trials

Microbiome Metabolites and Alcohol in HIV to Reduce CVD RCT

META HIV CVD
Start date: September 18, 2023
Phase: Phase 2
Study type: Interventional

Among people living with HIV, heavy drinking increases the risk of heart disease and death. Studies suggest that alcohol changes the number and kind of bacteria in your gut and these changes increase the risk of heart disease and death. This randomized controlled trial will determine whether a pill containing healthy gut bacteria can increase the number good bacteria in the gut, lower levels of inflammation, and lower the risk of heart disease and death.

NCT ID: NCT05192499 Recruiting - Asthma in Children Clinical Trials

Respiratory Dysbiosis in Preschool Children With Asthma: Predictive of a Severe Form

DREAM
Start date: February 4, 2022
Phase: N/A
Study type: Interventional

The prevalence of asthma in preschool children is between 11 and12%. Inhaled corticosteroid therapy is the main therapy used, however this treatment seems insufficiently effective in some children. Recent research in cystic fibrosis has made it possible to highlight pulmotypes corresponding to the different stages of pulmonary dysbiosis, and a predictive microbiological signature of an increased risk of early primocolonization to P. aeruginosa. These pulmotypes are the result of the so-called "enterotyping" analysis, a biostatistical method that makes it possible to stratify individuals according to the analysis of the microbiota. In the light of these data, it seems interesting to transcribe the concept of using a biomarker of the microbiota in the monitoring of a chronic lung disease such as asthma. The hypothesis is that there is respiratory dysbiosis causing corticosteroid resistance to treatment in children under 3 years of age with severe asthma.

NCT ID: NCT05176535 Recruiting - Clinical trials for Microbial Colonization

Determination of Vaginal Colonization and the Effect of an Oral Probiotic (PROSALVAG)

PROSALVAG
Start date: October 11, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to determine the efficacy of an oral nutraceutical with probiotics in restore vaginal health.

NCT ID: NCT05083572 Recruiting - Dysbiosis Clinical Trials

Effect of Probiotic on Gut Microbiome and Bacterial Translocation in Healthy Asian Volunteers

Start date: March 10, 2021
Phase: Phase 4
Study type: Interventional

Dysbiosis of the gut microbiome has been recognized to underlie the pathogenesis of various gastrointestinal conditions. Probiotics are known to exert beneficial effects on gut health and have great potential for use as microbiome interventions for gastrointestinal and metabolic diseases. While it is widely known that probiotic bacteria favourably alter the intestinal microflora balance, their other mechanisms of action have not been systematically characterized. The ability of probiotics to modulate dysbiosis may lead to reduced levels of endotoxaemia and oxidative stress. In this study, the investigators propose to examine the effects of 4-week Vivomixx treatment on the gut microbiome and bacterial translocation in healthy Asian volunteers with and without colonic lavage or antibiotic treatment. The study will also examine the same outcome parameters 4 weeks upon cessation of the product. The findings derived from the study will provide valuable insights into the microbiota changes associated with colonic lavage or antibiotic treatment, and the use of probiotic (Vivomixx). This has important clinical implications in designing treatment strategies in clinical practice such as the use of Vivomixx as microbiome interventions with antibiotics which are known to induce Clostridium difficile-associated diarrhoea, as well as in the therapeutic management of various diseases associated with dysbiosis.