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NCT ID: NCT01985152 Recruiting - Health Clinical Trials

A Phase Ⅰa Study of Azilsartan Trimethylethanolamine in Healthy Volunteers

Start date: September 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the Pharmacokinetics and safety of Azilsartan Trimethylethanolamine in healthy volunteers

NCT ID: NCT01877460 Completed - Health Clinical Trials

Sodium Alginate in Chocolate Milk, Satiety and Glycemic Control

Start date: January 2012
Phase: N/A
Study type: Interventional

This study compares the effects of isovolumetric (325 ml) preloads of chocolate milk supplemented with sodium alginates at incremental doses on inter-meal glucose levels, appetite scores and food intake in healthy adult men. The findings of this study will illustrate whether the addition of sodium alginate to chocolate milk will improve the glycemic properties of chocolate milk and will potentiate its satiating characteristics. This study will also elucidate whether sodium alginates, incorporated into chocolate milk, will influence glycemia, appetite sensations and food intake in a dose-dependent manner. It is hypothesized that there will be a synergy between milk and sodium alginate beyond either alone. When combined with milk components, sodium alginate is expected to improve glycemia and induce satiety more than does either milk alone or alginate alone.

NCT ID: NCT01762553 Completed - Health Clinical Trials

TEA for Families and Children: A Randomized Intervention Trial

Start date: May 2011
Phase: N/A
Study type: Interventional

The impact of HIV/AIDS is negatively influencing the affected families and their next generation. HIV is radiating through the extended families, shifting the life patterns not only for the parents living with HIV/AIDS (PLH), but also for their children, partners, and other family members. To help PLHs and their family members, the TEA intervention has been developed, refined and piloted in the previous study. The goal of this study is to implement the TEA intervention in a full scale to determine its efficacy and the potential for enhancing HIV policy and programs that support HIV-affected families to cope with the challenges in China in responding to the global HIV epidemic.

NCT ID: NCT01603888 Completed - Heart Disease Clinical Trials

Molecular Forms of Plasma and Urinary B-type Natriuretic Peptide and Its N-terminal Prohormone in Health and Disease in Pediatric Cardiology

Start date: January 2013
Phase: N/A
Study type: Observational

B-type natriuretic Peptide (BNP) is a cardiac hormone secreted from the cardiac myocytes in response to volume load. Plasma levels of BNP, as measured by immunoassay methods, are elevated in patients with heart diseases. However, the biological effects of BNP are blunted in heart failure and other cardiac conditions. Moreover, the peptide levels are also elevated in non cardiac conditions such as the neonatal period, sepsis and renal failure. Recent investigations suggest alteration of the peptide molecular structure in heart failure. These alterations may explain, at least partially, the reduced biological activities of BNP in heart failure. Immunoreactive BNP and NT-proBNP have been identified in human urine. It has been suggested that urinary BNP correlates with plasma BNP, and may serve as a non-invasive measure for this cardiac marker. It is unclear what BNP fractions are cleared in the urine in health and disease. The aim of the proposed studies is to elucidate precisely the molecular form of BNP in various disease and specific physiological states in plasma and urine of infants and children.

NCT ID: NCT01518270 Completed - Health Clinical Trials

Epidemiologic Analysis of Change in Eyelash Characteristics With Age in Healthy Women

Start date: December 1, 2011
Phase:
Study type: Observational

This study will asses epidemiologic changes in eyelash characteristics with increasing age.

NCT ID: NCT01484834 Completed - Health Clinical Trials

Comparison of Interventions to Promote Health in Workers

Start date: August 2011
Phase: Phase 0
Study type: Interventional

The goal of this research was to investigate different intervention strategies in the workplace and their impact on quality of life of workers from companies in the city of Londrina, Parana, Brazil. The interventions were composed by exercise in the workplace and educational interventions.

NCT ID: NCT01216605 Completed - Health Clinical Trials

Oxytocin and Emotion Recognition

Start date: November 2009
Phase: Phase 4
Study type: Interventional

The present study was designed to investigate the effects of a single dose of synthetic oxytocin on facial emotion recognition in healthy adult man. Pictures of emotional faces are presented very briefly for a few milliseconds in a backward-masking paradigm in order to vary the level of awareness. In a randomized placebo-controlled between-subject design, recognition performance is compared between a drug (24 IU oxytocin) and a placebo condition. We hypothesize that oxytocin enhances emotion recognition even for facial stimuli processed with limited awareness.

NCT ID: NCT01214278 Completed - Health Clinical Trials

Bioavailability of Different n-3 Fatty Acid Formulations

Start date: October 2010
Phase: Phase 4
Study type: Interventional

The aim of this study is to examine differences in short term bioavailability between four n-3 FA formulations in healthy males.

NCT ID: NCT01174576 Completed - Health Clinical Trials

Acute Effects of Coffee on Appetite and Inflammation Markers, Glucose Metabolism and Energy Intake

Start date: February 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate whether caffeinated and decaffeinated coffee consumption has acute effects on subjective appetite feelings, energy intake and biochemical markers related to appetite, inflammation and glucose metabolism compared to water consumption.

NCT ID: NCT01123772 Completed - Health Clinical Trials

Phase I Dose-Escalation Study to Evaluate Tolerability, Safety & PK of INO-8875 in Healthy Older-Adult Volunteers

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

The purpose of this study is to evaluate how tolerable and safe it is to give INO-8875 eye drops at different concentrations to normal older healthy adult volunteers for two weeks.