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Healthy Subjects clinical trials

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NCT ID: NCT01540734 Completed - Healthy Subjects Clinical Trials

Pharmacokinetic Study Investigating the Extent of Paracetamol Absorption From a New Formulation of Paracetamol Compared With Panadol®

Start date: December 2009
Phase: Phase 1
Study type: Interventional

A single dose pharmacokinetic study investigating two paracetamol formulations

NCT ID: NCT01540721 Completed - Healthy Subjects Clinical Trials

Pharmacokinetic Study Investigating the Extent of Paracetamol Absorption From a New Formulation of Paracetamol Compared With Panadol® Extend

Start date: December 2009
Phase: Phase 1
Study type: Interventional

This study will evaluate the pharmacokinetic profiles of experimental formulations of paracetamol.

NCT ID: NCT01530386 Completed - Healthy Subjects Clinical Trials

A Multicenter, Open-label Study to Determine the Effects of Lacosamide on Sleep in Healthy Subjects

Start date: January 2012
Phase: Phase 1
Study type: Interventional

The effects of Lacosamide, an antiepileptic drug, on sleep have not been formally evaluated. The present study is being conducted to assess the effects of Lacosamide on sleep quality in healthy subjects.

NCT ID: NCT01527669 Completed - Healthy Subjects Clinical Trials

The Pharmacokinetic Study of Red Yeast Rice Capsule Compared to Lovastatin Tablet in Healthy Subjects

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The objective of the study is to evaluate the pharmacokinetics of lovastatin and lovastatin acid of four 600 mg LipoCol Forte capsules compared to that of one 20 mg lovastatin Tablet after single oral administration in healthy subjects.

NCT ID: NCT01517087 Completed - Healthy Subjects Clinical Trials

Studying Motor Neuron Tests

Start date: February 1, 2012
Phase:
Study type: Observational

Background: - People with motor neuron disorders have changes in the parts of the brain that control movement. Some tests that are currently used to study these changes are magnetic resonance imaging (MRI) and transcranial magnetic stimulation (TMS). We don t know if MRI scans and TMS give the same results if done at different times in the same person. Researchers want to see if these tests produce different results if given to healthy adults on two separate occasions. Objectives: - To test the reliability of different tests of the brain used to study motor neuron disorders. Eligibility: - <TAB>Healthy individuals at least 35 years of age who have no history of neurological disorders and take no medications. - <TAB>Pregnant women may not participate. Design: - Participants will be screened with a medical history and physical exam. - Participants will have two testing visits 1 to 6 months apart. - The first visit will have three parts. The first part is a neurological exam to test strength, sensation, reflexes, and coordination of movement. The second part will be TMS tests. The third part will involve an MRI scan to study the parts of the brain that control movement. - At the second visit, participants will have MRI scanning only.

NCT ID: NCT01496677 Completed - Healthy Subjects Clinical Trials

Pharmacokinetics, Safety, and Tolerability of TR-701 Free Acid (FA) in Elderly Subjects

Start date: January 17, 2012
Phase: Phase 1
Study type: Interventional

To compare the pharmacokinetic (PK) profile of TR-700 in elderly subjects versus younger control subjects

NCT ID: NCT01495494 Completed - Healthy Subjects Clinical Trials

A Multiple Use Tolerability Study of a Breathe Right Nasal Strip Prototype

Start date: November 2009
Phase: Phase 1
Study type: Interventional

This study evaluated the safety & tolerability of two Breathe Right nasal strip prototypes. Prototypes were produced as an improvement to the currently marketed product.

NCT ID: NCT01491113 Completed - Healthy Subjects Clinical Trials

Pharmacokinetic (PK) Study in Japanese Non-epileptic Renal Impaired Patients

Start date: November 2011
Phase: Phase 4
Study type: Interventional

This is a human pharmacology, single-dose study to investigate the pharmacokinetics of orally administered Levetiracetam (LEV) in Japanese subjects with normal renal function and in Japanese subjects with various degrees of impaired renal function.

NCT ID: NCT01489696 Completed - Healthy Subjects Clinical Trials

A Study to Evaluate Cardiovascular Interactions Between Mirabegron and Tamsulosin

Start date: August 2010
Phase: Phase 1
Study type: Interventional

The study aims to compare blood pressure and pulse in male healthy subjects taking mirabegron and tamsulosin both alone and in combination.

NCT ID: NCT01487135 Completed - Healthy Subjects Clinical Trials

Phase 1 Study to Assess the Effects of EVP-6124 on the QT/QTc Interval in Healthy Subjects

TQT
Start date: December 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the effect of EVP-6124 at therapeutic and supratherapeutic concentrations on cardiac repolarization in healthy subjects.