Examples of using Crossover study in English and their translations into German
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Medicine
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Political
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Computer
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Programming
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Political
Crozz, VW presented a crossover study combining SUVs with electromobility.
Active-Controlled, 4-Week, Noninferiority, Blinded Crossover Study Study 1.
For this reason, the DIfE researchers investigated the effect of 50 g isomaltulose and50 g sucrose in a crossover study of 10 adults with type 2 diabetes.
The new urban crossover study ŠKODA VISION X and the‘Innovation Tunnel' provide an ideal framework for presenting visionary mobility ideas.
The supportive EUR-1008-M, conducted in the US, was a randomized, double-blind,placebo-controlled, crossover study of 34 patients, ages 7 to 23 years, with EPI due to CF.
In one placebo-controlled crossover study of 10 elderly subjects with mild cognitive impairment, treatment with 6 mg of melatonin led to improve sleep, memory, and mood in the elderly.
The effect of idelalisib(150 mg and 400 mg) on the QT/QTc interval was evaluated in a placebo-and positive-controlled(moxifloxacin 400 mg) crossover study in 40 healthy subjects.
The pharmacokinetic parameters derived from a crossover study of ADVATE in 100 previously treated patients≥ 10 years of age are listed in table 3 below.
Researchers of the University of Texas, USA, investigated the effects of THC(dronabinol) on the pain of 7 patients with spinal cord injury andneuropathic pain in a double-blind, crossover study.
In a double-blind, crossover study, the reduction in glycosylated haemoglobin levels after 12 weeks dosing was 0.37 percentage points with insulin lispro, compared to 0.03 percentage points for soluble insulin p 0.004.
The effect of rilpivirine at the recommended dose of 25 mg once daily on the QTcF interval was evaluated in a randomised, placebo and active(moxifloxacin 400 mg once daily)controlled crossover study in 60 healthy adults, with 13 measurements over 24 hours at steady-state.
In a randomized, crossover study with 20 healthy adult men, pharmacokinetics was investigated following inhalation of Ventavis(5 mcg iloprost) by the I-Neb AAD in comparison to the ProDose 5 mcg disk.
The effect of multiple doses of glycerol phenylbutyrate 13.2 g/day and 19.8 g/day(approximately 69% and 104% of the maximum recommended daily dosage) on QTc interval was evaluatedin a randomised, placebo- and active-controlled(moxifloxacin 400 mg), four-treatment-arm, crossover study in 57 healthy subjects.
A small double-blind, placebo-controlled, crossover study using the synthetic cannabinoid nabilone in patients with generalised and segmental primary dystonia found no significant reduction in dystonia following treatment with the cannabinoid.
Another randomised, double-blind, multiple- dose, comparator-controlled, two-way crossover study in 50 healthy volunteers showed that the pharmacokinetic profile of Nivestim was comparable to that of the reference product after subcutaneous administration.
In a crossover study in 60 healthy volunteers, intracellular lamivudine-TP pharmacokinetic parameters were similar(AUC24, ss and Cmax24, ss) or lower(Ctrough- 24%) for the lamivudine 300 mg once daily regimen compared to the lamivudine 150 mg twice daily regimen.
Pharmacokinetics of iloprost were investigated in a randomised, crossover study with 27 patients, stable on Ventavis 10 microgram/ml inhaled with I-Neb, following inhalation of single doses of 2.5 or 5 microgram iloprost using the Breelib or the I-Neb AAD nebuliser.
A double-blind, randomised, placebo-controlled crossover study has been conducted in which 114 patients who experienced on average 1 to 4 episodes of break through pain(BTP) per day while taking maintenance opioid therapy were entered into an initial open-label titration phase in order to identify an effective dose of PecFent Study CP043.
Science: Cannabis abuse Canadian researchers conducted a double-blind, placebo-controlled, crossover study with cannabis users, who at different occasions received a single dose of either THC(20 and 40 mg) or the cannabis extract Sativex(containing 10.8, 21.6 and 43.2 mg THC) or placebo.
All randomized, controlled trials of parallel-group design and randomized crossover studies that compared walking training with other interventions were included.
Of the 95 publications included, 80% were randomized controlled trials andthe remaining 20% were randomized crossover studies.