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Gut Microbiota clinical trials

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NCT ID: NCT04880083 Completed - Gut Microbiota Clinical Trials

Feeding Tolerance and Gut Maturation of Infants Consuming a Formula Rich in Glycoprotein

Start date: July 9, 2021
Phase: N/A
Study type: Interventional

This is a non-randomized, single-arm, open-label, prospective interventional study using a commercially available starter infant formula in healthy term formula-fed infants with a parallel group of healthy term breast-fed infants as reference group. Approximately 120 male and female infants (60 per group) who are 3-28 days old and are exclusively or predominately formula-feeding or breastfeeding will be enrolled.

NCT ID: NCT04501601 Completed - Gut Microbiota Clinical Trials

The Effect of Consuming on Body Composition and Blood Biochemistry Index

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

To assess the effect of consuming on body composition and blood biochemistry index

NCT ID: NCT04435548 Active, not recruiting - Gut Microbiota Clinical Trials

Westlake Gut Microbiome Study

Start date: September 1, 2021
Phase:
Study type: Observational

The Westlake Gut Microbiome study is a prospective cohort study. This project aims to characterize the gut microbiome among Chinese populations from different regions of China, and explore the relationships between gut microbiota and human health. Human fecal samples will be collected from the participants and muli-omics detection and analysis will be performed.

NCT ID: NCT04431960 Completed - Clinical trials for Cardiovascular Diseases

Blackcurrants Modify Gut Microbiota and Reduce Osteoporosis and CVD Risk

Start date: July 20, 2021
Phase: Phase 1
Study type: Interventional

Aim to evaluate the effects of blackcurrant supplementation on changes in gut microbiome, bone mass, and CVD risk factors in adult women.

NCT ID: NCT04399434 Recruiting - Gut Microbiota Clinical Trials

Gut Microbiota, SCFAs and Glucolipid Metabolism in Pregnant Women With Abnormal Fetal Size and Their Newborns

Start date: January 1, 2019
Phase:
Study type: Observational

Abnormal fetal size includes fetal growth restriction and fetal macrosomia. Onset is closely related to maternal nutrition metabolism. The specific correlation and mechanism is unclear, and there are no effective measures for early diagnosis and treatment. Previous study found that maternal gut microbiota participates in the material metabolism throughout the pregnancy. Insulin sensitivity in pregnant women, and intrauterine environment under abnormal blood glucose and lipid metabolism are important for the gut microbiota of newborns and even they grow up. However, changes in gut microbiota are the cause of the disease or the outcome is not yet clear. Short chain fatty acids (SCFAs) are produced from soluble dietary fibers in the diet by colon bacteriolysis. Studies have found that gut microbiota can regulate insulin sensitivity and glucose and lipid metabolism disorders through SCFAs. Therefore, this research group uses the gut microbiota as a new idea to studythe relationship of gut microbiota characteristics and level's change of SCFAs with glucolipid metabolism and insulin sensitivity in pregnant women with abnormal fetal size and their newborns through 16S-rRNA high-throughput sequencing, pyrosequencing, and gas chromatography-mass spectrometry, so we can reveal the role of gut microbiota in the pathogenesis of abnormal fetal size and explore targeted rational dietary adjustment and SCFAs reconstruction of gut microbiota to improve maternal and neonatal pregnancy outcomes.

NCT ID: NCT04355910 Recruiting - Obesity Clinical Trials

Intermittent Fasting in Nonalcoholic Fatty Liver Disease

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Although preliminary evidence suggests that intermittent fasting mimic-diet (IFD) exerts stronger effects on body weight and metabolic parameters, which may link obesity, non-alcoholic fatty liver disease (NAFLD) and major chronic diseases, compared with continuous calorie restriction (CCR), there is a lack of well-powered intervention studies. This randomized controlled trial will test whether IFD, operationalized as the "5:2 diet," has stronger effects on anthropometric and body composition characteristics, and circulating metabolic biomarkers than CCR and a control regimen in adults with NAFLD.

NCT ID: NCT04351841 Completed - Gut Microbiota Clinical Trials

To Investigate the Effect of Arabinogalactan on the Gut Microbiome in Adults

Start date: August 5, 2019
Phase: N/A
Study type: Interventional

Dietary fiber is an important nutrient that supports gastrointestinal function, as well as the maintenance of blood glucose and cholesterol. Additionally, it is suggested that dietary fiber may provide other health benefits, such as maintenance of healthy weight through effects on satiety. Furthermore, dietary fiber can improve health by modulating the microbial communities residing in human gut, particularly in the large intestine. The microbes in the gut modulate a wide variety of biological processes essential for health of the host. Currently, the average intake of fiber in the U.S. is ~40-50% below adequate intake levels. ResitAid, a Lonza's arabinogalactan, is a hemicellulose that is abundant in plants. Arabinogalactans including ResitAid are found in seeds, leaves, roots, and fruit of higher plants, such as cereals, beans, leeks, pear, corn, bark, and wheat. ResitAid, the arabinogalactan ingredient used in this study, is isolated from larch (Larix laricina) using a patented water-based extraction process. ResitAid has been designated as Generally Recognized as Safe (GRAS) by the U.S. FDA for multiple uses and has been used in numerous previous clinical studies in humans, with no significant safety issues observed at intakes of up to 30 g daily for up to 6 weeks. It was reported that 15 g and 30 g of different preparation of arabinogalactan could significantly increase certain microbial populations considered to be beneficial (e.g., Lactobacillus spp.). Nevertheless, more clinical evidence is needed to support the effect of ResistAid on the microbial composition in the gut. This study is designed to investigate the effect of daily consumption of 15 g of ResitAid on the gastrointestinal microbial profile and fecal short-chain fatty acid contents in healthy adults. Primary Objective: Modulation of the microbiome Secondary objectives: 1. Changes in Lactobacillus ssp. 2. Changes in Bifidobacterium ssp. 3. Changes in SCFA 4. Changes in bowel movement 5. Changes in the SF-36 questionnaire

NCT ID: NCT04333004 Not yet recruiting - NSCLC Clinical Trials

Analysis of Gut Microbiota in Patients With Brain Metastasis of Non-small Cell Lung Cancer Treated by Pembrolizumab Combined With Chemotherapy

Start date: April 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Analysis of Gut Microbiota in Patients With Brain Metastasis of Non-small Cell Lung Cancer Treated by Pembrolizumab Combined With Chemotherapy

NCT ID: NCT04316910 Not yet recruiting - Clinical trials for Postoperative Delirium

Characterisation of Gut Microbiota in Patients Undergoing Gastrointestinal Surgery With Postoperative Delirium (GIM-POD)

GIM-POD
Start date: July 19, 2023
Phase:
Study type: Observational

The study is a case-controlled observational trial. Sixty patients will be divided into 2 groups depending on whether postoperative delirium or not. This study aims to characterise the gut microbiota in patients undergoing gastrointestinal surgery with postoperative delirium. The CAM-ICU (Confusion Assessment Method for Intensive Care Unit) was used for delirium assessment.

NCT ID: NCT04303481 Completed - Gut Microbiota Clinical Trials

The Effect of Consuming Enzymes and Prebiotics on Body Composition and Blood Biochemical Index

Start date: August 10, 2019
Phase: N/A
Study type: Interventional

To assess the effects of consuming enzymes and prebiotics on improvement of weight loss and biochemical parameters