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NCT ID: NCT05922189 Not yet recruiting - Healthy Clinical Trials

The Effect of the SBS Decompression Technique on Gastrointestinal Symptoms During the Menstrual Cycle

Start date: September 1, 2024
Phase: N/A
Study type: Interventional

Determining the effects of a single application of the sphenobasilar synchondrosis (SBS) decompression technique, on gastrointestinal symptoms during the menstrual cycle is an area that lacks of evidence and proper studies. Therefore the investigators consider this an interesting topic to study.

NCT ID: NCT05920707 Recruiting - Healthy Clinical Trials

Common and Differentiated Representations Between Social Exclusion and Social Separation

Start date: April 20, 2023
Phase: N/A
Study type: Interventional

Explore the shared or separated neural mechanisms of social exclusion and social segregation and compare differential effects of AVP and OXT on these social interaction function.

NCT ID: NCT05919589 Recruiting - Healthy Clinical Trials

Evaluating Care Integration for Children With Special Health Care Needs v1.0

Start date: November 1, 2023
Phase:
Study type: Observational

The Evelina London Children's Hospital (ELCH) is planning to integrate care for children with special health care needs (CSHCN) using a package of support, including 1) family support workers to manage care coordination and support parents, and 2) 'navigation' packs outlining key services, for both the services users and providers. This study aims to explore the views and experiences of key stakeholders involved with these services, including the parents/caregivers of CSHCN, and professionals/staff team members. These will be explored using semi-structured qualitative interviews.

NCT ID: NCT05917002 Not yet recruiting - Healthy Clinical Trials

MPFC Theta Burst Stimulation as a Tool to Affect Rational Decision Making

Start date: August 1, 2024
Phase: Early Phase 1
Study type: Interventional

This is a study to investigate if a device that temporarily changes brain activity (repetitive transcranial magnetic stimulation, rTMS) might be used to change how healthy participants make decisions. This study involves 2 visits to MUSC that will each take between 2-3 hours. This study is not a treatment study, but it could help inform studies investigating treatment in the future. Participants in this study will be compensated for their time.

NCT ID: NCT05916560 Recruiting - Healthy Clinical Trials

A Study of LY3437943 in Participants With Impaired and Normal Liver Function

Start date: July 13, 2023
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to measure how much of LY3437943 gets into the bloodstream and how long it takes the body to eliminate it in participants with mild, moderate and severe impaired liver function compared to healthy participants with normal liver function. The safety and tolerability of LY3437943 will also be evaluated. The study may last up to 9 weeks for each participant including the screening period.

NCT ID: NCT05915871 Completed - Healthy Clinical Trials

Drug Interaction Study Between Tegoprazan, Bismuth, Amoxicillin and Clarithromycin

Start date: March 23, 2023
Phase: Phase 1
Study type: Interventional

To evaluate the pharmacokinetic interaction between tegoprazan and combination of Amoxicillin, Clarithromycin and bismuth in healthy adult volunteers.

NCT ID: NCT05915546 Completed - Healthy Clinical Trials

The Effect of Food on the Pharmacokinetics (PK) of Emraclidine in Healthy Adult Participants

Start date: June 8, 2023
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to evaluate the effect of food (a high-fat meal) on the pharmacokinetics of emraclidine and metabolite CV-0000364 following single oral dose administration in healthy adult participants.

NCT ID: NCT05914688 Completed - Healthy Clinical Trials

A Study to Compare Two Formulations of LY3209590 in Healthy Participants

Start date: June 26, 2023
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to compare the two formulations of LY3209590 in healthy participants. Study participants will be administered each formulation at separate study visits. Blood samples will be taken to compare how the body handles study drugs. The information about any adverse effects experienced will be collected and the tolerability of LY3209590 will also be evaluated. Screening is required within 28 days prior to enrolment. For each participant, the total duration of the clinical trial will be about 184 days including screening.

NCT ID: NCT05913635 Active, not recruiting - Healthy Clinical Trials

Effects of Time-Restricted Fasting on the Postprandial Glycemic Responses

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to investigate whether fasting timing has a significant effect on postprandial glycemic responses in healthy adults. The main questions it aims to answer are: 1. Whether fasting timing has a significant effect on postprandial insulin actions and plasma glucose concentration. 2. Whether fasting timing could modulate the glycemic metabolome and circadian rhythms in healthy individuals. Participants will get the two interventions: No-dinner: breakfast at 7.30 a.m., lunch at 1.00 p.m. and no dinner; No-breakfast: no breakfast, lunch at 1.00 p.m. and dinner at 8.00 p.m.

NCT ID: NCT05908474 Recruiting - Healthy Clinical Trials

The Effects of io Fibrewater Supplementation on Gut Health, Immunity and Metabolism in Overweight Adults

IOFW
Start date: April 25, 2023
Phase: N/A
Study type: Interventional

Despite availability of many alternative and conventional weight loss options, the prevalence of obesity increased from 15% in 1993 to 27 in 2015. In 2015, 68% of men and 58% of women in the UK were overweight or obese. Overweight and obesity increase the risk for comorbidities such as hypertension, dyslipidaemia, cardiovascular disease, type 2 diabetes and certain cancers. Hormonal regulation of appetite has been shown to influence body weight and body fat . Gut hormones secreted from the intestine are particularly important both in the regulation of appetite and blood glucose level, and recently the gut hormone Glucagon Like Peptide -1 (GLP-1) has been successfully targeted to treat both type 2 diabetes and obesity. Targeting the gut microbiota has been shown to influence gut hormones, in a way is likely to help treat or prevent obesity and type 2 diabetes. In past decades, considerable attention has been given to investigating the new applications of natural prebiotic polymers on gut microbiota composition. Moreover, recent trend in research indicates a bidirectional communication between the gut microbiota and the central nervous system through the microbiome-gut-brain axis (MGBA). Therefore an in vivo intervention feeding study is proposed performed with a variety of psychological and nutritional tests aiming to compare io fibrewater with an equivalent placebo control water and also highlight both cognitive function, emotional bias and response to appetite and also metabolic profiles of the gut microbiota.