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Healthy Volunteers clinical trials

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NCT ID: NCT03488082 Completed - Healthy Volunteers Clinical Trials

MRI Study of Saccadic Adaptation

Start date: October 17, 2018
Phase: N/A
Study type: Interventional

Accurate execution of our directed behaviors in the immediate environment allows the vast majority of our daily activities. Through the movements of our eyes and different parts of our body, we perceive, explore and act on our environment and can exchange and communicate with others. The mechanisms of sensorimotor adaptation of saccades (saccadic adaptation) contribute on the one hand to maintain the accuracy of saccades in the short, medium and long term, by opposing the deleterious effects of various physiological changes (development, aging), pathological or environmental (optical corrections). The aim of this study is to identify neuronal structures and networks involved in saccadic adaptation through the study of brain metabolic activation (BOLD) during the development of the adaptation of reactive saccades. The study will be organized in a single session with 3 runs. Each run include 4 blocks: 3 include the double-step target paradigm RND, U+, U-) and one without target jump (STA). The 'U+'/ 'U-'blocks include saccadic trials with forward/backward displacement of the target during a targeting saccade, the 'RND' block include saccadic trials with random target jump (forward or backward) and the 'STA' block are trials without displacement of the target. Each subject will make 12 repetitions of the 4 blocks.

NCT ID: NCT03488017 Completed - Healthy Volunteers Clinical Trials

Ocular Coil Drug Delivery Comfort Trial

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

The Ocular Coil is intended to provide drug delivery to the ocular surface. This study will evaluate the safety and tolerability of the placebo Ocular Coil in healthy subjects.

NCT ID: NCT03485755 Completed - Healthy Volunteers Clinical Trials

Pediatric Microbiome Study With Children Now Approximately 8-10 Years Old.

Start date: March 12, 2018
Phase:
Study type: Observational

Single site study involving Biological Mothers and their children approximately 8-10 years old to assess the predominant microflora and skin physiology.

NCT ID: NCT03483233 Completed - Healthy Volunteers Clinical Trials

Neural Bases of the Check Process

Check
Start date: November 23, 2018
Phase: N/A
Study type: Interventional

Effective exploration of the environment, check for information to improve one's own performance, are fundamental abilities of human cognition. These abilities are dependent on the process of cognitive control. However, they are clearly impaired and uncontrollable in certain behavioral disorders such as obsessive-compulsive disorder (OCD). Compulsive checks of these patients, spontaneously associated with a feeling of intense uncertainty, suggest disturbances of evaluative and metacognitive functions. However, no biological observations have yet been able to feed these hypotheses. The evaluation of decisions and actions involves the middle cingulate cortex (MCC) (which belongs to a cortico-subcortical network structurally and functionally altered in OCD patients). Cingulotomy has long been used as a therapy in severe OCD, with However, the precise part of the cingulate cortex that contributes to check (and its pathological forms) remains to be discovered. The purpose of this research campaign is to determine, through functional magnetic resonance imaging (fMRI) and electroencephalography (EEG) in healthy human subjects: 1. the location and role of the MCC region involved in normal check decision processes, 2. determine the identity of the entire network involved

NCT ID: NCT03482453 Completed - Healthy Volunteers Clinical Trials

A Study to Evaluate the Pharmacokinetics (PK), Safety and Tolerability of TAK-788 Followed by Evaluation of the Effects of a Low-Fat Meal on TAK-788 PK and Evaluation of Relative Bioavailability of TAK-788 Capsules in Healthy Participants

Start date: March 28, 2018
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the safety, tolerability of TAK-788 and to identify a tolerable single oral dose of TAK-788 administered as a drug-in-capsule (DiC) formulation, to characterize the effects of a low-fat meal on the PK of the TAK-788 administered as DiC formulation and to evaluate the bioavailability of a test (Process B) DiC of TAK-788 relative to a reference (Process A) DiC of TAK-788 in healthy participants.

NCT ID: NCT03478319 Completed - Healthy Volunteers Clinical Trials

A Study of ACE-2494 in Healthy Subjects

Start date: February 15, 2018
Phase: Phase 1
Study type: Interventional

The purpose of the study is to assess safety, tolerance, pharmacokinetic, and pharmacodynamics of single doses of ACE-2494 in healthy postmenopausal women.

NCT ID: NCT03478020 Completed - Healthy Volunteer Clinical Trials

Oral AQX-1125 and Combination Oral Contraceptive Drug-Drug Interaction Study

DDI-COC
Start date: November 22, 2017
Phase: Phase 1
Study type: Interventional

This is an open-label, fixed sequence, 4 cycle, drug-drug interaction (DDI) study of AQX-1125 in healthy female subjects on combination oral contraceptives (COC).

NCT ID: NCT03475485 Completed - Healthy Volunteers Clinical Trials

ID-Cap System Under Direct Observation

Start date: March 22, 2018
Phase: N/A
Study type: Interventional

The ID-Cap System is classified as an ingestion event marker (IEM), a Class II medical device. The system is intended to record time-stamped ingestions with the ingestible sensor, ID-Tag which transmits a signal to a wearable device, the ID-Cap Reader. In this study, 36 subjects will ingest capsules containing ingestible sensors while wearing the Reader and being observed in a clinic setting.

NCT ID: NCT03472313 Completed - Healthy Volunteers Clinical Trials

Assessment of the Biodistribution and Safety of [18F]MNI-958 in Healthy Subjects

Start date: November 14, 2017
Phase: Phase 1
Study type: Interventional

The overall goal of this protocol is to evaluate the biodistribution of [18F]MNI-958 also known as APN-0000455 or PM-PBB3, as a tau targeted radiopharmaceutical.

NCT ID: NCT03471130 Completed - Healthy Volunteer Clinical Trials

Definitive QT Study With MT-8554

MT-8554 DQT
Start date: April 23, 2018
Phase: Phase 1
Study type: Interventional

This is a study to definitively assess the effects of MT 8554, adjusted for placebo, on the change of the QT interval corrected for heart rate (HR) using the Fridericia formula (QTcF) from Baseline in healthy adult subjects