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Healthy clinical trials

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NCT ID: NCT02345304 Withdrawn - Healthy Clinical Trials

Effect of BI 1181181 on Midazolam, Warfarin, Omeprazole and Digoxin

Start date: March 2015
Phase: Phase 1
Study type: Interventional

To assess the influence of different dose strengths of BI 1181181 on single dose kinetics of midazolam (CYP3A4 probe drug), warfarin (CYP2C9 probe drug), omeprazole (CYP2C19 probe drug) and digoxin (P-gp probe drug)

NCT ID: NCT02341976 Withdrawn - Healthy Clinical Trials

Whole Body Vibration Training for Pelvic Floor Muscle

Start date: January 2015
Phase: N/A
Study type: Interventional

To study which position on the whole body vibrator machine would stimulate the pelvic floor muscles.

NCT ID: NCT02312752 Withdrawn - Healthy Clinical Trials

Intra-epidermal Stimulation (IES) of Small Nerve Fibers (A-delta Fibers)

IES
Start date: December 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether a particular type of nerve fibers, A-delta fibers, can be tested in an Electromyography (EMG) lab on a routine basis. Normal, healthy volunteers will be enrolled in this study.

NCT ID: NCT02289274 Withdrawn - Healthy Clinical Trials

Study to Compare Pharmacokinetic Characteristics of Eperisone and Aceclofenac With NVP-1203

NVP-1203
Start date: November 2019
Phase: Phase 1
Study type: Interventional

The purpose of this study is to compare the pharmacokinetics of NVP-1203 and coadministration of aceclofenac and eperisone HCl SR.

NCT ID: NCT02210299 Withdrawn - Healthy Clinical Trials

TEXTO : Total EXposure To Organic Pollutants

TEXTO
Start date: September 2014
Phase: N/A
Study type: Interventional

People are, especially in industrialized countries, exposed to a growing number of ubiquitous chemical substances. It thus increases human exposure pathways: diet, inhalation, soil and dust dermal contact…), notably for semi-volatile organic compounds. Diet is generally sought to contribute the most to total exposure for many chemicals, the relative contribution of each pathway is nevertheless poorly described, and can be different among populations. This is in particularly the case For young children, who can be more exposed via the environment, because of frequent contact with object and dust and hand to mouth behaviors. Children are in addition considered more sensitive to chemical risk due to their maturating systems. In this context, the objective of this project is to characterize the young children's exposure to a particular class of semi volatile organic compounds. It will encompass the relative contribution of different pathways to the external dose, and to try to match the internal and external doses with a physiologically based pharmacokinetic (PBPK) model for molecules for which it is possible. The present demand concerns a feasibility study on 2 children, for Perfluorinated Alkylated Substances (PFAS), used in numerous consumer products.

NCT ID: NCT02187393 Withdrawn - Healthy Clinical Trials

Determining in Vitro Properties of Epithelial Cells From Individuals With Genetic Variants Associated With Idiopathic Pulmonary Fibrosis

Start date: July 2015
Phase: N/A
Study type: Observational

The investigators are trying to understand the role of specific genes in the function of airway surface cells. The investigators know that there are some common genetic markers that are associated with various lung diseases. However, most people with these genetic markers never develop any evidence of lung disease, so it is not understand how or if these markers play a role in disease. Investigators are asking healthy people to provide three (3) tubes of blood as well as a sample of cells from their nose. Investigators will use the blood sample to provide genetic information (specifically, presence or absence of alleles known to be associated with pulmonary fibrosis). Nose cells from individuals with the genetic markers that investigators are studying will be grown in the the lab to allow investigators to learn more about how the cells respond to various forms of environmental stress, such as exposure to cigarette smoke. The goal of this study is to understand how specific genes affect airway cell function.

NCT ID: NCT02175238 Withdrawn - Healthy Clinical Trials

Relative Bioavailability of BI 691751 Administered With and Without Food to Healthy Male Subjects

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

The primary objective of this trial is to investigate the relative bioavailability and pharmacokinetics in plasma and whole blood of BI 691751 administered as a single dose with and without food in healthy male subjects.

NCT ID: NCT02133482 Withdrawn - Healthy Clinical Trials

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Rising Oral Doses of BI 639667

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

The primary objective of this trial is to investigate the safety and tolerability of BI 639667 in healthy male subjects following oral administration of single rising doses. Secondary objectives are the exploration of the pharmacokinetics (PK) including dose proportionality as well as investigation of linearity and pharmacodynamics (PD) of BI 639667 after single dosing and the assessment of the PK/PD relationship.

NCT ID: NCT02116595 Withdrawn - Healthy Clinical Trials

Urine pH and Diet Net Acid Load

Start date: January 2015
Phase: N/A
Study type: Interventional

Presently, the gold standard for testing diet acid intake is a urine collection done for many hours, usually 24 hours, which must be analyzed in a research lab for "net acid excretion". So, getting information about diet acid intake is difficult. Many people have suggested doing a much simpler test, which is checking the pH of the urine when you wake up. But, no one has studied if this simpler method is a valid method for estimating the 24 hour net acid excretion. Diet acid load may be important in many diseases associated with aging, such as loss of bone and muscle, and the development of kidney disease.

NCT ID: NCT02114671 Withdrawn - Healthy Clinical Trials

A Study to Investigate the Phototoxic Potential of Faldaprevir

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

To investigate the potential of Faldaprevir to induce skin phototoxicity, immediate or delayed type, to UV light and visible light in healthy male and female subjects. To investigate the degree, wavelength dependency, severity, pigmentation and morphology of the phototoxic effects. The persistence of the phototoxic susceptibility will be explored following cessation of study medication. Within a sunscreen sub-study, the efficacy of commercially available high factor sunscreen will also be assessed in terms of its potential to prevent any phototoxic skin responses seen. The safety and tolerability of Faldaprevir will also be assessed.