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Healthy Subjects clinical trials

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NCT ID: NCT01199523 Completed - Healthy Subjects Clinical Trials

A Study to Evaluate the Effect of Oral Mirabegron on the Heart in Healthy Males and Females

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

The objective of this study is to evaluate the effect of repeat oral dosing of mirabegron on ECG (electrocardiogram) measurements.

NCT ID: NCT01182129 Completed - Healthy Subjects Clinical Trials

4 mg Nicotine Polacrilex Gum and Swedish Portion Snus

SMWS06
Start date: March 2006
Phase: Phase 1/Phase 2
Study type: Interventional

Fifteen healthy smokers are given single doses of General Onyx 1 g portion snus and General White 1g portion snus, respectively, and one piece of Nicorette 4 mg chewing gum. Serial blood samples are drawn before (0), 2, 4, 8, 16, 24, 30, 45, 60 minutes, 1.5, 2, 4, 6 and 8 hours after administration for determination of nicotine. Mean + SD extracted dose of nicotine from each preparation will be estimated. The percentage extracted of the nicotine content will be calculated. Cmax and Tmax will be estimated. A comparison to Nicorette 4 mg chewing gum will be made. The dose absorbed into the systemic blood circulation (AUC) in relation to the dose following the 4 mg Nicorette chewing gum will be calculated. Self-reports of subjective effects will be obtained up to 30 minutes after the test product is administered using a 100 mm visual analogue scale (VAS) anchored with "not at all" to "extremely". Study hypothesis is that Cmax and AUC of Nicorette 4 mg chewing gum and Swedish snus are similar.

NCT ID: NCT01181505 Completed - Healthy Subjects Clinical Trials

STUDY The Effect of HNF-4A G60D Variant on the In VIVO CYP2D6 Activity By Tolterodine Pharmacokinetic Study

HNF4a
Start date: January 2007
Phase: Phase 1
Study type: Interventional

This study was to investigate the pharmacokinetics of tolterodine, substrate of CYP2D6 in healthy subject in relation to the presence of HNF-4A G60D variant.

NCT ID: NCT01176201 Completed - Healthy Subjects Clinical Trials

14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man

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

This is an open-label study to determine the ADME (Absorption, Disposition, Metabolism and Excretion) of 14C labeled SLV337 after a single dose of an oral suspension.

NCT ID: NCT01175746 Completed - Healthy Subjects Clinical Trials

The Effect of Nicardipine on Kidney Function During Orthognathic Surgery Under Hypotensive Anesthesia

Start date: August 2010
Phase: N/A
Study type: Interventional

Since nicardipine is known to protect kidney function, nicardipine infusion will result in better renal parameters measured in this study.

NCT ID: NCT01174485 Completed - Healthy Subjects Clinical Trials

Effects of Liposuction and Exercise Training on Metabolism, Lipid Profile and Adiposity in Women

Start date: August 2010
Phase: Phase 0
Study type: Interventional

Liposuction is the most popular aesthetic surgery in Brasil and worldwide. Evidence showing that adipose tissue is a metabolically active tissue led to the suggestion that liposuction could be a viable method for the improvement of metabolic profile through the immediate loss of adipose tissue. Studies about the effects of liposuction on metabolic profile are conflicting. A few studies report the improvement of insulin sensitivity, inflammatory markers and lipid profile, others observe no changes and a few report the worsening of metabolic profile. In addition, animal studies show a compensatory growth of intact adipose tissue in response to lipectomy. Physical exercise improves insulin sensitivity, lipid profile, inflammatory balance, adipose tissue distribution and increases or preserves free fat mass. Therefore, liposuction and physical exercise seem to act on similar tissues of the body. To the investigators knowledge, there are no studies about the associated effects of liposuction and exercise in humans. However, one can suggest that exercise training associated with liposuction could: [1] attenuate or block the possible fat recovery or compensatory growth; [2] block or reverse the possible harmful effects of liposuction; or [3] exert an additive or synergistic effect to the possible beneficial effects induced by liposuction on metabolic and hormonal profile and inflammatory balance.

NCT ID: NCT01172951 Completed - Healthy Subjects Clinical Trials

Nutrigenomics Investigation of the Body's Metabolic Response to 2 Different Meal Challenges

MECHE
Start date: December 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the biological response to a metabolic stress, given in the form of a high carbohydrate or fat meal in normal weight, overweight and obese individuals and to further explore these responses using novel metabolomic, proteomic, transcriptomic and genotyping techniques.

NCT ID: NCT01169506 Completed - COPD Clinical Trials

Sublingual Tonometry to Assess Tissue Perfusion in Patients With Chronic Obstructive Pulmonary Disease (COPD)

subton
Start date: August 2009
Phase: N/A
Study type: Interventional

Sublingual positioning of a silicon capillary system is applied. After 15 min, while the individual is in resting position with closed mouth and normal tidal breathing through the nose is performed, the silicon capillary system is connected to a capnometer and CO2 tension is measured. The investigators hypothesis is that this setup offers a non-invasive assessment of ventilatory efficiency with similar accuracy as arterial PCO2.

NCT ID: NCT01141504 Completed - Healthy Subjects Clinical Trials

Effect of Oral Adenosine-triphosphate (ATP) on Human Muscle Performance

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

Adenosine-triphosphate (ATP) serves as the sole energy source for muscle contraction. Therefore human performance of brief maximal exercise is limited, in part, by the availability of ATP to the contracting muscle. Because muscle ATP storage is small (enough to sustain maximal exercise for less than 1 second), factors that enhance either storage or resynthesis of ATP may have a positive impact on repeated muscle contractions. The current study will test the hypothesis that increasing ATP availability to muscle via oral supplementation will improve performance of repeated high intensity exercise as measured by a) work performed in each of the three 50 contraction fatigue tests, b) sum of total work performed, and c) percentage decrement in total work from the first to third third 50 contraction test.

NCT ID: NCT01124084 Completed - Healthy Subjects Clinical Trials

The Factors Affecting Intentions of Medical Staff to Use Personal Health Record in Northern Hospitals of Taiwan

Start date: March 2010
Phase: N/A
Study type: Observational

Application of health information technology be able to solve a lot of problems of medical management, and effective actions to achieve the purpose of medical care. The "Personal Health Record" (PHR), so that patients can have, access and update their health records and share health information to a new healthcare provider can avoid the duplication of a clinic procedures, reduce medical costs and time, and can make an appointment online, tracking vaccinations, check drug allergy, master with health-related information such as exercise, diet condition, and have no time constraints to the hospital clinic. In the future, PHR is expected to reduce medical errors, reduce costs, effective use of medical resources. Purpose of this study is to understand the impact to the staff's attitude and intention when they use the PHR, and to explore the medical records of personal health awareness and intention to use the relevant factors, the research result will be a reference to government authority or medical institutions in order to promote personal health record system in Taiwan. In this study, there will include the medical staff of three hospitals in Taipei, the Technology Acceptance Model (TAM model) based structured questionnaire will be used, questionnaire had tested by validity and reliability. The electronic questionnaires will be used, and apply the software SPSS and Amos17.0 descriptive and inferential statistical analysis.