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Healthy Volunteers clinical trials

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NCT ID: NCT02792686 Completed - Healthy Volunteers Clinical Trials

ABX464 First in Man Study

Start date: March 2014
Phase: Phase 1
Study type: Interventional

This study is an open label, parallel group, single ascending dose, exploratory study performed in a single site (Centre Cap, Montpellier, France).

NCT ID: NCT02792647 Completed - Healthy Volunteers Clinical Trials

A Study of Multiple Oral Doses of IX-01 in Healthy Male Subjects

Start date: May 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate the safety and tolerability of IX-01 after multiple doses, and to determine the PK of IX-01 and activity of CYP3A4.

NCT ID: NCT02792010 Completed - Healthy Volunteers Clinical Trials

Feasibility and Reproducibility of T1 Rho MRI in the Evaluation of Hip Cartilage

CARHAT02
Start date: May 2015
Phase: N/A
Study type: Interventional

Hip osteoarthritis is a frequent and invalidating disease. Early detection of cartilage modifications could provide better patient treatment. The T1rho MRI sequence allows the quantification of the cartilage signal that is correlated to modifications of the cartilage matrix, notably of the proteoglycans. The primary objective is to evaluate normal values of hip cartilage in vivo using T1rho MRI in healthy subjects and the reproducibility of the measurements. T1rho and T2 mapping sequences were acquired twice during the same session with 30 minutes interval to see if values were modified after a 30 minutes delay in a supine position. The secondary objective was to assess the correlation between T1rho and T2 values.

NCT ID: NCT02790411 Completed - Healthy Volunteers Clinical Trials

Adjustment Exploratory Protocols and Functional Evaluation of New Non Invasive Devices in Healthy Volunteers

MAP-EFNI
Start date: May 21, 2013
Phase: N/A
Study type: Interventional

Parameters, sequences or paradigms optimisation in view of data quality and relevancy improvement.

NCT ID: NCT02789007 Completed - Healthy Volunteers Clinical Trials

Effects of Parabolic Flight on Spatial Cognition and Hippocampal Plasticity

HypoCampus
Start date: March 2016
Phase: N/A
Study type: Interventional

The main objective of this experiment is to assess the impact of parabolic flight on (1) spatial memory and orientation, (2) the changes in brain structure and function, and particularly the hippocampal formation, and (3) biochemical markers of stress and neuroplasticity. A preliminary study will be performed with the aims (1) to test during weightlessness hardware used to administer visuo-spatial testing and (2) to determine the optimal body posture for testing under microgravity conditions (i.e. body posture for which change in visuo-spatial testing induced by weightlessness is maximal). The main criteria are: - Structural and functional changes of brain evaluated by fMRI; - Cognitive performance, and specifically spatial cognition using a series computer-based tasks. - Key neurotrophins determined in venous blood samples The criteria used in the preliminary experiment is visuo-spatial performance evaluated with a computer-based test assessing spatial cognition. The investigators hypothesize that hippocampal structure and function, and particularly the dentate gyrus, will be altered after parabolic flight compared to ground based controls. Specifically, the 3 tested hypotheses are: - Parabolic flight induces changes in hippocampal structure; - Weightlessness induces changes in cognitive performance, and specifically spatial cognition; - There is a correlation between changes in hippocampal structure and changes in visuo-spatial memory performance. - There is a correlation between changes in hippocampal structure and changes in key neurotrophins. The hypothesis tested during the preliminary experiment is that body posture affects the changes in spatial cognition performance.

NCT ID: NCT02785978 Completed - Healthy Volunteers Clinical Trials

Pilot Study to Evaluate ActiMyo Measured Activity in Parkinson Disease Patients & Healthy Volunteers

Pre-QuantiPark
Start date: June 2016
Phase: N/A
Study type: Interventional

Pre-QuantiPark is a pilot study to evaluate the reliability and responsiveness of ActiMyo measured activity in PD patients. The purpose of the study is to provide validation of the ActiMyo, an innovative home-recording device enabling use in clinical trials and as an innovative tool for PD patient care.

NCT ID: NCT02779361 Completed - Healthy Volunteers Clinical Trials

Effect of Tea Consumption on Steroid Profile in Healthy Volunteers

Start date: January 2016
Phase: Phase 1
Study type: Interventional

Open label phase I clinical trial in healthy volunteers designed to assess changes on steroid profile after green tea consumption.

NCT ID: NCT02777554 Completed - Healthy Volunteers Clinical Trials

A Study to Evaluate the Pharmacokinetic Exposure of 2 Formulations of Apremilast in Healthy Adults

Start date: August 17, 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the relative bioavailability of apremilast once-daily formulation relative to a twice daily formulation when administered as multiple doses (Part 1), and when administered as a single dose under fasting and fed conditions (Part 2). Information on safety and tolerability will also be obtained.

NCT ID: NCT02777151 Completed - Healthy Volunteers Clinical Trials

Study of Safety, Tolerability, and Pharmacokinetics of REGN3470-3471-3479 in Healthy Adult Volunteers

Start date: May 27, 2016
Phase: Phase 1
Study type: Interventional

This is a Phase 1, randomized, double-blind, placebo-controlled, dose escalation study evaluating the safety, tolerability, pharmacokinetics (PK) and immunogenicity of REGN3470-3471-3479 in healthy adult volunteers.

NCT ID: NCT02775175 Completed - Healthy Volunteers Clinical Trials

Influence of a Modified Ramadan Fasting on Health and Well-being in Healthy Muslims - a Randomised Controlled Trial

Ramadan_16
Start date: May 2016
Phase: N/A
Study type: Interventional

In this study the investigators will test the impact of a modified Ramadan Fasting regimen on health and well-being. The 2016 Ramadan is around summer solstice in Germany making it one of the most challenging fasting periods for participating Muslims. The modified Ramadan Fasting consists of educational components around fasting, and advice for nutritional modifications in order to support health and well-being during Ramadan, while the control group will continue to fast as usual. The investigators will measure not only body weight/fat but also include measures of psychological well-being, and spiritual practice, and serum markers for blood lipids, and blood sugar. With this trial the investigators aim to determine, whether such modifications around Ramadan will be beneficial for health and well-being.