Examples of using Crossover study in English and their translations into Portuguese
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All participants received both the extract andthe placebo at different times crossover study.
In a crossover study Stacey et al. compared direct laryngoscopy and jaw trust to aid Fiberoptic intubation.
Minutes after Kentera application was evaluated in a single-dose randomised crossover study N=16.
In a single dose, crossover study of desloratadine, the tablet and the syrup formulations were found to be bioequivalent.
Patients and methods: this was a randomized double blind crossover study with duration of 13 months.
In a single dose, crossover study of desloratadine, the tablet and the syrup formulations were found to be bioequivalent.
Eight healthy dogs, weighing 15.4± 2.9 kg, was used in a blind,randomized and crossover study.
A short-term crossover study comparing fast bubbling with minimum bubbling did not find any difference in blood gases.
The influence of weather on the risk of pain exacerbation in patients with knee osteoarthritis: A case crossover study.
The crossover study design allowed patients to be used as their own controls, thereby enhancing homogeneity of the responses.
Subjects were randomly allocated to groups in a crossover study, subjects were randomly allocated an order in which treatments were received.
The crossover study design was used in order to allow the subjects to participate in all three mask trials consecutively.
Links et al. compared the effects of lithium and desipramine in a six-week crossover study, involving a small sample of borderline patients n=17.
This randomized crossover study was carried out at the outpatient clinic of the"League of Diabetes", Discipline of Endocrinology, HC-FMUSP.
Plasma bimatoprost andtimolol concentrations were determined in a crossover study comparing the monotherapy treatments to GANFORT treatment in healthy subjects.
Celich& Galon, in a crossover study with elderly living in the city of Cruzaltense/RS, have found similar results, with prevalence of 40.7% of CP among males.
Methods: it was perfomed a randomized and crossover study was conducted, with hypertensives, with no other comorbidities, 40-65 years old.
A crossover study was carried out with FM female patients aged between 35 and 65 years, in the period from January to June 2010, in the Clínica Escola de Fisioterapia, Universidade Potiguar UNP, Natal, Brazil.
Methods: nine men with recent mi(54.2 years)were randomized in a crossover study/ open and participated in two sessions of exercises with and without nitrate supplementation from the beet juice~ 8 mmol of no3.
This was a quantitative, crossover study, conducted with 68 hospitalized children in a pediatric health care unit Unidade de Atenção a Saúde da Criança- UASC of a university hospital, and located in the northeastern region of Brazil.
This is a descriptive, correlational and crossover study carried out in the Application School Professor Vande de Souza Ferreira, Petrolina.
In another crossover study, an acute exposure protocol consisting of 10 sequential puffs, 30 s apart, was used in order to compare four experimental conditions: an EC brand with a 16-mg nicotine cartridge; another EC brand with a 16-mg nicotine cartridge; own brand cigarettes; and an unlit cigarette placebo.
The prevalence of CP in this study was similar to findings of the crossover study carried out in Londrina/PR where, from 71 male elderly, 52% have reported CP with similar pain location for lower limbs 31.4%, however lower for low back pain 30.2.
In a double-blind crossover study comparing nabilone and dihydrocodeine for neuropathic pain, both drugs had no satisfactory results.
This is a quantitative,descriptive, crossover study carried out in a NICU of a non-for-profit hospital size IV, from the Northwestern region of the state of Rio Grande do Sul.
This double-blind subject and statistician crossover study was developed in the Microbiological Testing Laboratory LEM of the Department of Medical-Surgical Nursing of the University of São Paulo School of Nursing.
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.
In an open-label, non-randomized, fixed-sequence, 3-period, 3-treatment, crossover study to evaluate the effect of multiple doses of ketoconazole on the single dose PK of naloxegol, co-administration of ketoconazole and naloxegol resulted in a 12.9 fold(90% CI: 11.3-14.6) increase in naloxegol AUC and a 9.6-fold increase in naloxegol Cmax(90% CI: 8.1-11.3), compared to when naloxegol was administered alone.
But there are many circumstances in which such crossover studies are simply not possible.
In single-dose crossover studies of Aerius 5 mg orodispersible tablets with Aerius 5 mg conventional tablets, the formulations were bioequivalent.