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Personal Satisfaction clinical trials

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NCT ID: NCT02256904 Active, not recruiting - Clinical trials for Personal Satisfaction

RSA and Clinical Comparison of Anatomical and Mechanical Alignment in Total Knee Replacement

Start date: April 13, 2015
Phase: N/A
Study type: Interventional

Current practice in orthopedics is to recommend TKA implantation with the femoral and tibial components perpendicular to their mechanical axis. Therefore, current surgical technique does not replicate natural knee anatomy and biomechanics. An alternative alignment method that attempts to replicate the kinematics of the knee is " kinematic alignment ". The principle behind kinematic alignment is placement of the TKA components so that the orthogonal 3-D orientation of the 3 axes that describe normal knee kinematics is restored to that of the prearthritic knee. Theoretical benefits of kinematic alignment include less ligamentous release to balance the knee intra-operatively, more rapid recovery, better range of motion (ROM), less post-operative pain, better knee biomechanics, and improved patient satisfaction. However, a major concern is that there are no mid- or long-term data on implant survivorship (absence of loosening) in TKA based on "anatomical" implantation. The investigators propose to compare the clinical results of TKA implanted with mechanical alignment (standard practice) to kinematic alignment, in a double-blind, randomized trial.

NCT ID: NCT02036697 Terminated - Clinical trials for Hemodynamic Instability

Hemodynamic Effects of Low Dose Spinal Anesthesia for Cesarean Section

Start date: November 2013
Phase: N/A
Study type: Interventional

We propose to study the effects on hemodynamics (blood pressure, cardiac output, and central venous pressure) of two doses of bupivacaine for spinal anesthesia during cesarean section: a higher dose of 12 mg to a lower dose of 4.5 mg. We will examine recovery times, incidence of hypotension, and compare pain control and maternal satisfaction during and after cesarean section. We hypothesize that low dose bupivacaine spinal anesthesia will provide equivalent anesthesia for cesarean section compared to conventional dose bupivacaine, with less hypotension, faster recovery time, and enhanced maternal satisfaction. Maternal satisfaction will be assessed by self-reported pain scores, incidence of nausea and vomiting, shivering, and ability to interact with baby in the OR.

NCT ID: NCT02011035 Completed - Clinical trials for Personal Satisfaction

Evaluating the Clinical Efficacy and Safety of Colflex

Start date: November 2013
Phase: Phase 1
Study type: Observational

This study is designed to test the safety and efficacy of Colflex, an oral spray created by Innotech Nutrition, on human subjects to measure changes on frequency/duration of colds and sore throats, as well as dental and oral health changes.

NCT ID: NCT01874132 Completed - Osteoporosis Clinical Trials

Study of the Long-term Effects of Exercise on Heath Indicators in Older People

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

Cardiovascular diseases (CVD) represent the most frequent cause of death among the elderly population. Hypertension, unfavorable lipid profile, obesity and physical inactivity are among the main risk factors for CVD. In contrast, mortality from CVD is inversely related to levels of physical activity, and is lower in individuals who exercise and have higher functional fitness levels. Thus, the Centers for Disease Control and Prevention, the American College of Sports Medicine, and the American Heart Association have recommended 20-30 min of moderate-to-vigorous aerobic training for the elderly, preferably every day or at least 3 days a week in the case of vigorous exercise.The same organizations also suggest the inclusion of resistance training in order to improve functional fitness. Therefore, the purpose of this study was to compare different exercise modalities in long-term changes of CVD risk factors and physical fitness among older adults.

NCT ID: NCT01641861 Completed - Dental Caries Clinical Trials

A Comparative Study of Papacarie® and the Conventional Method for Dental Caries Treatment

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

The purpose study are to evaluate the efficacy of Papacarie® for caries removal in comparison to the conventional drilling method.

NCT ID: NCT01373541 Completed - Health Behavior Clinical Trials

Effect of InFatâ„¢ Product on Stool Biochemistry and Stool Characteristics in Formula-fed Term Infants in China

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

The purpose of this study is to determine the effect of infant formula with high percentage of palmitic acid at the sn-2 position (InFatâ„¢) on improving fat absorption and general gastrointestinal tolerance in Chinese formula-fed term infants.

NCT ID: NCT01316029 Completed - Signs and Symptoms Clinical Trials

Safety/Effectiveness Study of a Single Session of Laying-on-of-hands in Various Settings in Japan

SELH
Start date: February 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine the symptomatic changes after a single session of laying-on-of-hands in various settings, and to evaluate optimal conditions for the outcomes.

NCT ID: NCT00874068 Completed - Clinical trials for Personal Satisfaction

The Effects of Dietary Palmitic Acid Triacylglyceride Position on Bone Strength Parameters in Infants

InFat_002
Start date: February 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of high sn-2 palmitic acid based infant formula on bone strength parameters.