نتایج جستجو برای: in a randomized crossover design

تعداد نتایج: 20481955  

2008
Pranab K. Sen Vernon M. Chinchilli

When conducting a paired 2 × 2 crossover design, each subject is paired with another subject with similar characteristics. The pair is then randomized to the same sequence of two treatments. That is, the two subjects receive the first experimental treatment, and then they cross over and receive the other experimental treatment(s). The paired 2× 2 crossover design that was used in the Beta Adren...

Journal: :Diabetes care 2005
Yogish C Kudva Ananda Basu Gregory D Jenkins Guillermo M Pons Lori L Quandt Julie A Gebel Debra A Vogelsang Steven A Smith Robert A Rizza William L Isley

OBJECTIVE Multiple daily insulin injection programs are commonly accompanied by considerable glycemic variation and hypoglycemia. We conducted a randomized crossover design clinical trial to compare glargine with ultralente insulin as a basal insulin in type 1 diabetes. RESEARCH DESIGN AND METHODS To determine whether the use of glargine insulin as a basal insulin would result in a comparable...

Introduction and purpose: Massage and dry cupping are two pre-competition modalities that are used to help improve athletes’ performance. The purpose of this study was to investigate the effects of pre-exercise massage and dry cupping on selected skill-related fitness components, and psycho-cognitive functioning in athletes. Materials and Methods: Twelve male athletes (age: 22.25±1.8 years, wei...

Introduction and purpose: Post-activation potentiation (PAP) is the phenomenon by which muscular performance is enhanced in response to a conditioning stimulus. The purpose of this study was to compare the effects of PAP induced by resisted, accelerated and traditional plyometric with and without caffeine ingestion on competitive judokas performance. Materials and Methods: In a randomized, c...

D Beiki M Amini M Pirali R Dowlatabadi

The bioavailability of two dipyridamol tablet formulations of (Dipyridamole from Tolidaru and Persantin from Boehringer) was compared in 14 healthy male volunteers who received a single dose of 25 mg of the test (T) and the reference (R) products in a randomized balanced 2-way crossover design. Plasma samples were obtained over a 16 h interval and dipyridamole concentrations determined by HPLC ...

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