Results for randomized translation from Czech to English

each visit to darkwood is unique, as all locations and events are randomized.
each visit to darkwood is unique, as all locations and events are randomized.

a randomized trial. journal of the american medical association 293:43-53
a randomized trial. journal of the american medical association 293:43-53.

a total of 34% of participants who had been randomized at the time of the event attended.
a total of 34% of participants who had been randomized at the time of the event attended.

a randomized controlled trial of the effect of school food and dining room modifications on classroom behaviour in secondary school children.
a randomized controlled trial of the effect of school food and dining room modifications on classroom behaviour in secondary school children.

in a cross-over randomized study, the effect of heat on lymph drainage was evaluated in the treatment of leg lymphedema.
in a cross-over randomized study, the effect of heat on lymph drainage was evaluated in the treatment of leg lymphedema.

the efficacy and safety of dermagraft in improving the healing of chronic diabetic foot ulcers: results of a prospective randomized trial.
the efficacy and safety of dermagraft in improving the healing of chronic diabetic foot ulcers: results of a prospective randomized trial.

a randomized clinical trial. jama 2006, 296: 2329-2335. přejít k původnímu zdroji... přejít na pubmed...
a randomized clinical trial. jama 2006, 296: 2329-2335. go to original source... go to pubmed...

2. foster, g.d. a další (2003) a randomized trial of a low-carbohydrate diet for obesity.
foster gd et al (2003) a randomized trial of a low-carbohydrate diet for obesity.

those randomized to the treatment group were offered the 12 month intervention immediately after randomization, while those randomized to the control condition were offered the intervention after a 12-month delay.
those randomized to the treatment group were offered the 12 month intervention immediately after randomization, while those randomized to the control condition were offered the intervention after a 12-month delay.

popis k další podpoře hodnocení poměru prospěchu a rizik se žadatel zavazuje poskytnout chmp k posouzení 48- týdenní data o bezpečnosti a účinnosti z probíhající studie fáze iii, protokol 018 (a multicenter, double- blind, randomized, placebo- controlled study to evaluate the safety and antiretroviral activity of mk- 0518 in combination with an optimized background therapy (obt), versus optimized background therapy alone, in hiv- infected patients with documented resistance to at least 1 drug in each of the 3 classes of licensed oral antiretroviral therapies) a protokol 019 (a multicenter, double- blind, randomized, placebo- controlled study to evaluate the safety and antiretroviral activity of mk- 0518 in combination with an optimized background therapy (obt), versus optimized background therapy alone, in hiv- infected patients with documented resistance to at least 1 drug in each of the 3 classes of licensed oral antiretroviral therapies).
description to further support the benefit risk assessment, the mah has provided the chmp with the 48-week safety and efficacy data from the ongoing phase iii protocol 018 (a multicenter, double-blind, randomized, placebo-controlled study to evaluate the safety and antiretroviral activity of mk-0518 in combination with an optimized background therapy (obt), versus optimized background therapy alone, in hiv- infected patients with documented resistance to at least 1 drug in each of the 3 classes of licensed oral antiretroviral therapies) and protocol 019 (a multicenter, double-blind, randomized, placebo- controlled study to evaluate the safety and antiretroviral activity of mk-0518 in combination with an optimized background therapy (obt), versus optimized background therapy alone, in hiv-infected patients with documented resistance to at least 1 drug in each of the 3 classes of licensed oral antiretroviral therapies) for review.