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NCT ID: NCT04398719 Recruiting - Healthy Clinical Trials

CBD-Microglia PET Study

Start date: May 7, 2021
Phase: Early Phase 1
Study type: Interventional

This study aims to examine the effect of cannabidiol (CBD) pre-treatment on brain microglial activation in healthy human subjects. Secondarily, this study aims to examine the effect of cannabidiol (CBD) pre-treatment on central pain-sensitization in healthy human subjects.

NCT ID: NCT04349137 Recruiting - Healthy Clinical Trials

Cause-effect Relationships Between Brain Networks and Bimanual Coordination in Older Adults

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

In this study, high-definition dual-site transcranial alternating current stimulation (i.e., non-invasive brain stimulation) will be applied to boost the fronto-parietal network during a bimanual coordination task in healthy young and older adults. Previous studies indicated that this network is important in initial motor learning, possibly through its role in spatial working memory. Therefore, stimulation will be applied during both a pure spatial working memory test, and during a bimanual coordination task. It is also shown that healthy older adults do not engage spatial working memory brain regions during motor learning, which is related to worse motor learning. Therefore, the investigators will investigate whether this type of stimulation can improve bimanual motor learning in healthy older adults.

NCT ID: NCT04343612 Recruiting - Healthy Clinical Trials

Different Montages of Transcranial Direct Current Stimulation Tongue Strength

Start date: May 7, 2020
Phase: N/A
Study type: Interventional

20 healthy subjects will be split into 4 groups. Each group will receive one of the following tDCS montages : anodal, bilateral, cathodal or placebo Subjects will receive 2mA for 20 mins of their attributed tDCS. The evaluation is a maximal strength test measured with the IOPI and will take place prior to, immediately following and 30 minutes after stimulation

NCT ID: NCT04325009 Recruiting - Healthy Clinical Trials

Bioequivalence Study Between "Dong-A Atorvastatin Tab" and "Lipitor Tab"

Start date: March 30, 2020
Phase: Phase 1
Study type: Interventional

An Open-Label, Randomized, 2-sequence, 4-period, Fasting Condition, Single-dose, Per Oral, Cross-over Study to Evaluate the Bioequivalence between "Dong-A Atorvastatin 80mg Tab" and "Lipitor 80mg Tab" in Healthy Volunteers

NCT ID: NCT04320706 Recruiting - Healthy Clinical Trials

Oral Oxytocin Modulation of Responses to Emotional Stimuli

Start date: February 20, 2020
Phase: N/A
Study type: Interventional

The main aim of the study is to investigate whether orally administered oxytocin (24IU) can modulate neural and behavioral responses to positive and negative valence stimuli during basal (emotional scenes) and higher order (facial stimuli) emotional processing.

NCT ID: NCT04319068 Recruiting - Healthy Clinical Trials

Sodium Storage in Singaporeans

SSIS
Start date: July 2, 2019
Phase:
Study type: Observational

The overarching hypothesis of this study is that the kidney and the skin form an integrative network for water conservation, where Na+ storage is utilized to prevent body water loss, even at the expense of increased cardiovascular risk. The aim of this project is to characterise skin and muscle Na+ storage in a cohort designed to prospectively measure cardiovascular outcomes in Singaporeans, in order to determine whether humans with increased tissue Na+ storage have increased cardiovascular risk. To gain a better understanding of the mechanisms behind Na+ storage, the investigators will also test the hypothesis that participants with mutations of the skin protein filaggrin, who have increased water loss through the skin, will have increased skin Na+ storage and higher blood pressure levels.

NCT ID: NCT04299490 Recruiting - Healthy Clinical Trials

Effects of Experimental Sleep Disturbances on Receptor Function of Study Drug

Sleep-MOR
Start date: November 11, 2020
Phase: Phase 2
Study type: Interventional

The overall goal of this project is to determine whether common sleep disturbance patterns, sleep continuity disturbance (SCD) and Sleep Fragmentation (SF), alter cerebral study drug receptor availability, drug-based analgesia, and drug abuse liability. The investigators specifically aim to: 1) evaluate whether experimental SCD and/or SF alter resting or pain-evoked receptor binding potential in brain regions associated with pain inhibition; 2) examine whether SCD and/or SF alters the analgesic response and abuse liability profile of a study medication; and 3) determine whether receptor binding potentials in brain regions of interest are associated with study medication analgesia and abuse liability. The investigators will also evaluate the extent to which associations differ by sleep condition or sex.

NCT ID: NCT04297865 Recruiting - Healthy Clinical Trials

Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of CJ-15314 Phosphate in Healthy Male Subjects

Start date: February 24, 2020
Phase: Phase 1
Study type: Interventional

This study aims to evaluate safety, tolerability, pharmacokinetics and pharmacodynamics of CJ-15314 phosphate in healthy male subjects.

NCT ID: NCT04297761 Recruiting - Healthy Clinical Trials

Cardiovascular Effects of Exposure to Wood Smoke in Healthy Human Adults

MASKOFF
Start date: May 25, 2021
Phase: N/A
Study type: Interventional

MASKOFF Clinical Trials 8/22/23 Brief Summary: Purpose: The study is designed to investigate cardiovascular effects of young healthy human subjects exposed to wood smoke. Participants: Approximately 80 young (18-35 years old) healthy subjects to complete. Procedure (methods): After consenting to participate in the study, subjects will be exposed first to filtered air and on the next exposure day to approximately 500 µg/m^3 wood smoke. Both exposures will be 2 hours long with alternating 15 min of exercise (cycle ergometer) and 15 min rest period. The exercise level will be adjusted to achieve approximately 12 L/min/m^2 minute ventilation. Venous blood samples and measurements of lung, cardiac and vascular function will be made prior to and immediately following each exposure. Induced sputum samples and nasal epithelial lining fluid will be collected approximately 24 hours post each exposure.

NCT ID: NCT04280419 Recruiting - Healthy Clinical Trials

An Investigation of the Effect of Environmental Factors on Respiratory Muscle Endurance Test Results in Healthy Individuals

Start date: February 28, 2019
Phase:
Study type: Observational

This study aims to investigate the effect of music as an environmental factor on respiratory muscle endurance in healthy individuals.