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NCT ID: NCT05222022 Completed - Healthy Clinical Trials

Engineering Evaluation of an Eye Movement Monitor Device

Start date: February 18, 2022
Phase: N/A
Study type: Interventional

The objective of the engineering evaluation is to verify and validate the design of an eye movement monitor device, the Retitrack, for recording, viewing, measuring, and analyzing temporal characteristics of fixation and saccadic responses in human eyes when viewing a visual stimulus. This engineering evaluation is not an applicable clinical trial. This is a design validation of the mechanism of action of the device to measure eye movement. This is not a clinical trial to evaluate the effect of an intervention on biomedical or other health-related outcomes.

NCT ID: NCT05221918 Enrolling by invitation - Healthy Clinical Trials

A Study to Compare CSF Flow Metrics Across Platforms

Start date: September 14, 2022
Phase:
Study type: Observational

The purpose of this research is to find out more about detecting movement of CSF (fluid around the brain) with MRI. Researchers are doing this research study to find out how measurements of CSF movement differ among MRI machines and how image quality is changed by reducing the scan time.

NCT ID: NCT05221242 Enrolling by invitation - Healthy Clinical Trials

Clinical Trial on Ceramic Partial Laminate Veneers With Different Luting Agents

Start date: January 4, 2021
Phase: N/A
Study type: Interventional

Partial laminate veneers is a type of dental restoration made of a glass-matrix ceramic used to restore small teeth fractures, or to correct morphology defects of teeth (i.e.: diastema, conoid teeth or small misalignment). As tooth surface reduction, or tooth preparation is not needed for this type of restoration, it can be considered as a non-tooth preparation minimally invasive procedure. As non-preparation is required for the restoration with ceramic partial laminate veneers, bonding relies on adhesion between the intaglio surface of the ceramic restoration and the tooth surface, which in most of the cases is enamel. For this purpose, many light-curing resin cement materials are available for bonding procedures. Nowadays, pre-heated resin composites are available as a resin luting material which has been indicated for laminate veneers and partial indirect posterior restorations. As pre-heated resin composite has not been yet studied for partial laminate veneers, the objective of this randomized split mouth clinical trial, is to evaluate the survival of ceramic partial laminate veneers when bonded with two different resin composite luting agents.

NCT ID: NCT05219799 Recruiting - Healthy Clinical Trials

Sex Disparities in Hypoxic Vasodilation and Impact of Obesity

Start date: March 14, 2023
Phase: Early Phase 1
Study type: Interventional

The purpose of this project is to examine key mechanisms contributing to sex-differences in hypoxic vasodilation and the impact of obesity, with particular emphasis on the sympathetic nervous system.

NCT ID: NCT05219682 Active, not recruiting - Healthy Clinical Trials

Changes in Brain Activity During Mirror Therapy and Virtual Reality Therapy

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

The purpose of this study is to compare electroencephalographic activity in upper limb rehabilitation with mirror therapy and virtual reality rehabilitation.

NCT ID: NCT05219448 Active, not recruiting - Healthy Clinical Trials

Reducing Sugared Fruit Drinks in Alaska Native Children

Start date: September 6, 2022
Phase: N/A
Study type: Interventional

This study in Alaska will test whether providing sugar-free alternatives to sugared fruit drinks and introducing education and social support will help families and children to reduce the amount of sugared fruit drinks consumed (measured through the primary outcome of added sugar intake).

NCT ID: NCT05218460 Recruiting - Healthy Clinical Trials

Evaluation of Methodological and Technical DEvelopmeNts to Improve the Quality and Comfort of Magnetic Resonance Imaging Exam on Voluntary Subjects

EDEN
Start date: May 23, 2022
Phase: N/A
Study type: Interventional

The EDEN study will make it possible to evaluate one or more development phases (from design to validation through optimization) of a method or a technique on voluntary subjects, in normal or pathological condition.

NCT ID: NCT05213481 Completed - Healthy Clinical Trials

Tepotinib Drug-Drug Interaction Study With Carbamazepine in Healthy Participants

Start date: December 15, 2021
Phase: Phase 1
Study type: Interventional

The purpose of this study was to assess the effect of multiple doses of carbamazepine on single- dose tepotinib pharmacokinetics in healthy participants. Study details include: Study Duration: up to about 10 weeks; Treatment Duration: single dose of tepotinib on Days 1 and 26, 25 days of treatment with carbamazepine (Days 8 to 32); Visit Frequency: residence in the Clinical Research Unit from Days -1 to 4 and Days 25 to 29, ambulatory daily visits from Days 5 to 24 and 30 to 33, and one ambulatory visit on Day 39.

NCT ID: NCT05212402 Completed - Healthy Clinical Trials

Assessing the Effects of a Cannabidiol Derived From Hemp Supplement in Healthy Adults

Start date: January 18, 2022
Phase: N/A
Study type: Interventional

The purpose of this prospective, randomized, double-blind, placebo-controlled trial is to assess the physiological, biochemical, and psychometric impacts of a brand-specific hemp-derived cannabidiol product in a sample of healthy adults.

NCT ID: NCT05211973 Completed - Healthy Clinical Trials

Geriatric Anorexia Study 2.0

GAS2
Start date: March 28, 2022
Phase:
Study type: Observational

Reduction in appetite and/or food intake among older individuals is referred to as anorexia of aging (AOA, also known as Geriatric Anorexia). AOA is linked with myriad comorbidities associated with aging, contributes significantly to adverse health consequences in old age, and has been used as a predictor of morbidity and mortality. The overall aim of this study is to compare feasibility of body weight, body fat, body composition and activity assessments in elderly subjects in long-term care (LTC), nursing home, or assisted living facilities. This will be accomplished through the use of questionnaires in addition to devices that evaluate movement, body composition, and body weight.