Примери за използване на Two randomised на Английски и техните преводи на Български
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diagnostic procedures was evaluated in two randomised, double-blind, placebocontrolled multicentre clinical trials.
The efficacy and safety of cinacalcet for the treatment of secondary HPT in paediatric patients with ESRD receiving dialysis was evaluated in two randomised controlled studies
The safety of Mimpara for the treatment of secondary HPT in paediatric patients with ESRD receiving dialysis was evaluated in two randomised controlled studies
have been assessed in two randomised, double-blind, cross-over,
Results through 48 weeks from two randomised, phase 3 double-blind studies comparing tenofovir disoproxil to adefovir dipivoxil in adult patients with compensated liver disease are presented in Table 3 below.
considering that the study protocols of the drug utilisation study and of the two randomised clinical trials are conditions to the marketing authorisation,
The efficacy and safety of Vemlidy in patients with chronic hepatitis B are based on 48- and 96-week data from two randomised, double-blind, active-controlled studies,
Efficacy in adult patients with pulmonary arterial hypertension Two randomised, double-blind, multi-centre,
Efficacy of Lyxumia was also assessed in two randomised, open-label, active-controlled study(versus exenatide
The safety and efficacy of Eylea were assessed in two randomised, multi-centre, double-masked,
Results through 48 weeks from two randomised, phase 3 double-blind studies comparing tenofovir disoproxil fumarate to adefovir dipivoxil in patients with compensated liver disease are presented in Table 2 below.
excluding patients with isolated anterior uveitis, in two randomised, double-masked, placebo-controlled studies(UV I and II).
96-week data from two randomised, double-blind, active-controlled studies, GS-US-380-1489(n= 629)
CD4 counts have been investigated in two randomised, multicentre, controlled studies(TORO 1
excluding patients with isolated anterior uveitis, in two randomised, doublemasked, placebo-controlled studies(UV I and II).
In each of two randomised, placebo-controlled trials, PROWESS
In each of two randomised, placebo-controlled trials, PROWESS
Adalimumab 40 mg every other week was assessed in 393 patients in two randomised, 24 week double-blind,
Baseline characteristics were balanced between the two randomised dose groups, except for marked differences in the mean value of baseline 24-hour UFC(1156 nmol/24 h for
Two randomised, double-blind, multi-centre,