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NCT ID: NCT05737082 Completed - Healthy Clinical Trials

A Study to Evaluate the Pharmacokinetics and Safety Between HCP2201 and Co-administration of Each Component in Healty Male Volunteers

Start date: March 30, 2023
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the pharmacokinetic characteristics and safety between HCP2201 and co-administration of each component in fasting condition in healthy male volunteers.

NCT ID: NCT05736029 Recruiting - Healthy Clinical Trials

Predicting Responsiveness in Oncology Patients Based on Host Response Evaluation During Anti Cancer Treatments, Using Multiomics

PROPHETIC
Start date: November 7, 2022
Phase:
Study type: Observational

The goal of this exploratory study is understand the mechanisms of response to immunotherapy in Non-Small Cell Lung Cancer patients. The investigators are going to search for correlation between specific biological features and response to immunotherapy, and to use those associations for developing an algorithm enabling to identify patients that could benefit from the immune check inhibitor based anti cancer treatment. Patients will provide biological samples before and during their treatment, and clinical data will be collected.

NCT ID: NCT05734534 Recruiting - Healthy Clinical Trials

Effects of BFR Interventions in Healthy Individuals and Individuals With COPD

Start date: March 1, 2023
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate the effect of different blood flow restriction (BFR) interventions on muscle function and adaptations both in healthy well-trained individuals and individuals diagnosed with COPD.

NCT ID: NCT05733364 Active, not recruiting - Healthy Clinical Trials

Effect of 4 Weeks Supplementation of a Combination of Vitamin Bs and Taurine on Mental Performance in Healthy Adults

Start date: March 8, 2023
Phase: N/A
Study type: Interventional

To evaluate the efficacy of the intervention in improving Motivation. To evaluate the efficacy of the intervention in improving Fatigue, Motivation/Vigor, Focus/Sustained Attention and blood levels of B vitamins and taurine.

NCT ID: NCT05732649 Recruiting - Healthy Clinical Trials

Improving Visual Perception and Visuo-motor Learning With Neurofeedback of Brain Network Interaction.

NF-BrainNet
Start date: May 1, 2023
Phase: N/A
Study type: Interventional

Neuroscience has long focused on understanding brain activity during task performance. As a result, current training methods aim to maximize brain activation during a trained task. However, new evidence shows that this may not be an efficient way to go. Human subjects achieve maximum performance only when the brain network is in a state of high spontaneous interaction and communication between brain regions before training or, in other words, in a state of high "network communication." In this case, minimal effort is required during the task. This requires new learning strategies aimed at inducing higher network communication prior to task execution. The investigators have previously shown that healthy people can learn to increase network communication of motor areas (i.e., the areas that control movement) when they receive real-time feedback on their current activity, which is known as neurofeedback. In neurofeedback, subjects receive continuous feedback about the state of their brain activity in a present moment. Through this feedback, they can learn to change their own brain activity. The aim of the present study is to validate neurofeedback as a new treatment approach for inducing high network communication at rest (i.e., when participants are not engaged in a task), and to test whether this heightened network communication can enhance visual perception and motor learning.

NCT ID: NCT05731908 Completed - Healthy Clinical Trials

A Study to Test How BI 690517 is Taken up in the Body of People With and Without Liver Problems

Start date: February 21, 2023
Phase: Phase 1
Study type: Interventional

The main objective of this trial is to assess the effect of mild and moderate hepatic impairment (Child-Pugh classification A and B) on the pharmacokinetics, safety, and tolerability of BI 690517 in comparison with a control group with normal hepatic function.

NCT ID: NCT05730179 Completed - Healthy Clinical Trials

Pain Inhibitory Effects of a Single Painful Mechanical Stimulus Compared to Multiple and Multiple at Different Locations

Start date: February 15, 2023
Phase: N/A
Study type: Interventional

The objective is to estimate the effects on pain thresholds of a single painful mechanical stimulus compared to multiple and multiple stimuli at different locations.

NCT ID: NCT05730166 Completed - Healthy Clinical Trials

Pain Inhibitory Effects of Other Pain Induced by Mechanical Pressure at Different Intensities

Start date: February 15, 2023
Phase: N/A
Study type: Interventional

The objective is to estimate the effects on pain thresholds of a painful mechanical stimulus on the upper trapezius at moderate intensity compared to mild intensity or non-painful.

NCT ID: NCT05730127 Completed - Healthy Clinical Trials

Pain Inhibitory Effects of Other Pain Induced by Mechanical Pressure Compared to Electrical Stimulation and Cold Water.

Start date: February 15, 2023
Phase: N/A
Study type: Interventional

The objective is to estimate the effects on pain thresholds of a painful mechanical stimulus on the upper trapezius compared to a painful electrical stimulus and a diffuse noxious stimulus using the cold water hand immersion test.

NCT ID: NCT05729685 Completed - Healthy Clinical Trials

Aerobic Adaptations With Various Training Methods

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The goal of this intervention study is to compare the adaptations after a 6-week training period between an intense continuous and a high-intensity interval training program performed under iso-effort conditions on aerobic performance parameters in young healthy adults. The main question it aims to answer are if the intense continuous and a high-intensity interval training programs will induce similar adaptations in maximal (VO2max and PTV) and submaximal (critical velocity, lactate threshold parameters and running economy) aerobic performance parameters. Participants will be ere randomly assigned either to an intense continuous training group (CON) or to a high-intensity interval training group (INT). The training program will comprise of 14 training sessions performed over a 6-week period.