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NCT ID: NCT05279339 Recruiting - Healthy Clinical Trials

Subjective and Objective Changes in Muscle-stiffness

Start date: February 21, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate muscle stiffness in relation to delayed on-set muscle soreness following exercise and to investigate how well the change in muscle stiffness correlates with the subjective experienced degree of stiffness.

NCT ID: NCT05277636 Completed - Healthy Clinical Trials

Acute Effects of R- and S-MDMA in Healthy Subjects

R-S-MDMA
Start date: October 1, 2022
Phase: Phase 1
Study type: Interventional

Racemic ±3,4-methylenedioxymethamphetamine (MDMA) is a psychoactive substance and prototypical empathogen acutely inducing feelings of heightened mood, empathy, trust and closeness to others. These acute subjective effects of MDMA may be helpful to assist psychotherapy and MDMA is currently investigated in phase 3 trials as a possible treatment in post-traumatic stress disorder.

NCT ID: NCT05277090 Not yet recruiting - Healthy Clinical Trials

Bowel Preparation May Lead to a Higher Feasibility of Intestinal Infection

Start date: March 15, 2022
Phase: Early Phase 1
Study type: Interventional

An adequate bowel preparation is essential for a high quality of colonscopy. Nowdays, polyethyleneglyco is considered the most safe drug for bowel preparation, and is widely used around the world. However, previous study illustrated that bowel preparation by polyethyleneglyco could lead to qualitative changes in the intestinal microbiota both in mice and human. This study is aimed to investigate wether the changes in the intestinal microbiota could lead to a higher rate of intestinal infection.

NCT ID: NCT05275660 Completed - Healthy Clinical Trials

A Study to Assess the Safety, Tolerability, and Pharmacokinetics of HFB30132A Against COVID-19 in Chinese Healthy Adults

Start date: May 9, 2021
Phase: Phase 1
Study type: Interventional

The purpose of this study is to examine the safety and tolerability of HFB30132A when it is given by single intravenous infusion in Chinese healthy participants.

NCT ID: NCT05274659 Active, not recruiting - Healthy Clinical Trials

A Study to Evaluate the Safety and Tolerability of KJ103 in Healthy Adults

Start date: May 31, 2022
Phase: Phase 1
Study type: Interventional

This is a randomized, single-blinded, placebo controlled, single ascending dose phase I study to evaluate the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) and immunogenicity of KJ103 in healthy subjects.

NCT ID: NCT05273203 Recruiting - Healthy Clinical Trials

The Influence of Football Training as a medicine_FIM_UTH

FIM
Start date: January 31, 2022
Phase: N/A
Study type: Interventional

The purpose of this randomized controlled study will be to inestigate the relationship between recreational football training at various training volumes and the health responses of middle-aged participants at high risk for metabolic and / or cardiovascular disease.

NCT ID: NCT05272683 Completed - Healthy Clinical Trials

Drug-drug Interaction Study With GLPG3667 and Itraconazole in Healthy Subjects

Start date: February 28, 2022
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to determine the effect of itraconazole on the amount of GLPG3667 that gets into the blood when the 2 drugs are administered together compared to when GLPG3667 is administered alone.

NCT ID: NCT05271656 Terminated - Healthy Clinical Trials

Evaluation of C-Scan Capsule in Identifying Subjects With Elevated Risk of Colon Polyps

Start date: May 10, 2022
Phase: N/A
Study type: Interventional

The main objective of the study is to determine the ability of the C-Scan system to identify subjects who are at elevated risk for colon polyps. This will be evaluated by comparing the C-Scan data to colonoscopy data. The C-Scan procedure is therefore performed before the colonoscopy procedure, in order to compare these tests and evaluate the C-Scan system's effectiveness. During the C-scan procedure, Subjects will be asked to come for an appointment in a clinic, during this appointment, the C-Scan Track will be placed on the participant's back. The participant will then be asked to swallow the C-Scan capsule whereafter they are free to continue their routine. Participants will start intake of fiber pills 5 days, and contrast agent 48 hours prior to C-Scan capsule ingestion and will continue intake up to the capsule's natural excretion. A standard colonoscopy procedure will be performed within 60 days following C-Scan Cap ingestion.

NCT ID: NCT05265806 Completed - Healthy Clinical Trials

The Effects of Oxytocin Treatment on Social Touch

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

The main aim of the study is to investigate the modulatory effects of oxytocin (24IU) administration on the affective processing of touch manipulated differently in gentle caress-like stroke vs. social massage with a moderate pressure.

NCT ID: NCT05265780 Completed - Healthy Clinical Trials

Effect of Kinesiotaping on Elbow Joint Proprioception

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

assessing the effects of kinesiotape application on elbow joint proprioception