What is the translation of " A RANDOMIZED " in Croatian?

Examples of using A randomized in English and their translations into Croatian

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A randomized clinical trial confirming this phenomenon is Yun2010npe.
Kliničke studije koje potvrđuju ovu pojavu je Yun2010npe.
And 3 are English sentences, but2 is a randomized set of characters with no meaning in English.
I 3 su rečenice na engleskom jeziku,no 2 je nasumičan set znakova koji u engleskom jeziku nema značenje.
A randomized, active controlled, long term study demonstrated that efficacy was maintained throughout a 1-year treatment period.
Randomizirano, aktivno kontrolirano dugoročno ispitivanje pokazalo je da je djelotvornost održana kroz jednogodišnje razdoblje liječenja.
The immunogenicity of IXIARO administered in a rapid vaccination schedule was evaluated in a randomized, observer-blind, phase 3 study.
Imunogenost cjepiva IXIARO primijenjenog prema brzom rasporedu cijepljenja procijenjena je u randomiziranom ispitivanju faze 3, slijepom za promatrača.
To be able to conduct a randomized, controlled trial, lots of perforations will need to occur.
Moći provesti randomizirani kontrolirani suđenje, puno perforacije treba da se dogodi.
HIV-positive, paediatric patients,aged 2 through 18 years, were studied in a randomized, open-label, multicenter study trial 1182.14.
HIV-pozitivni pedijatrijski bolesnici, u dobi 2 do 18 godina,bili su uključeni su u randomizirano, otvoreno, multicentrično kliničko ispitivanje ispitivanje 1182.14.
To be able to conduct a randomized, controlled trial, lots of perforations will need to occur.
Da bi mogli da sprovedu randomizirano, kontrolisano ispitivanje, mora se dogoditi mnogo perforacija.
The safety and efficacy of Soliris in PNH patients with haemolysis were assessed in a randomized, double-blind, placebo-controlled 26 week study C04-001.
Sigurnost i djelotvornost primjene lijeka Soliris u bolesnika s PNH-om procijenjene su u randomiziranom, dvostruko slijepom, placebom kontroliranom ispitivanju u trajanju od 26 tjedana C04-001.
To be able to conduct a randomized, controlled trial, lots of perforations will need to occur.
Da bi se moglo obaviti randomizirano, kontrolirano ispitivanje, morat će se dogoditi mnogo perforacija.
The efficacy and safety of Cimzia was assessed in DMARD-naïve adult patients with active RA in a randomized, placebo-controlled, double-blind clinical trial C-EARLY.
Djelotvornost i sigurnost Cimzije se ocjenjivala u odraslih bolesnika s aktivnim RA koji prethodno nisu bili liječeni DMARD-ovima u randomiziranom, placebom kontroliranom, dvostruko slijepom kliničkom ispitivanju C-EARLY.
Study 4 was a randomized, double-blind clinical study assessing ulipristal acetate 5 or 10 mg.
Ispitivanje 4 bilo je randomizirano, dvostuko slijepo kliničko isptivanje u kojem se ocjenjivao ulipristalacetat od 5 ili 10 mg.
The efficacy and safety of Tarceva as maintenance after first-line chemotherapy for NSCLC was investigated in a randomized, double-blind, placebo-controlled trial BO18192, SATURN.
Djelotvornost i sigurnost lijeka Tarceva u terapiji održavanja nakon prve linije kemoterapije raka pluća nemalih stanica ispitivale su se u randomiziranom, dvostruko slijepom, placebo kontroliranom ispitivanju BO18192, SATURN.
Study 02507 was a randomized, double-blind, placebo-controlled, multicenter clinical study in 40 patients with GD1.
Ispitivanje 02507 bilo je randomizirano, dvostruko slijepo, placebom kontrolirano, multicentrično kliničko ispitivanje na 40 bolesnika s GD1.
The efficacy and safety of methylnaltrexone bromide in the treatment of opioid-induced constipation in patients with chronic non-cancer pain were demonstrated in a randomized, double-blind, placebo-controlled study Study 3356.
Djelotvornost i sigurnost metilnaltreksonbromida u liječenju konstipacije uzrokovane opioidima u bolesnika s kroničnom nemalignom boli dokazane su u randomiziranom, dvostruko slijepom, placebom kontroliranom ispitivanju ispitivanje 3356.
Study 2 was a randomized, controlled, multicenter study comparing the Zevalin therapeutic regimen versus treatment with rituximab.
Ispitivanje 2 bilo je randomizirano, kontrolirano, multicentrično ispitivanje radi usporedbe terapijskog protokola Zevalina i liječenja rituksimabom.
A total of 234 subjects aged 1 to 17 years were treated in a randomized, double-blind, multi-centre, placebo controlled parallel group, dose ranging study.
U randomiziranom, dvostruko slijepom, multicentričnom, placebom kontroliranom ispitivanju raspona doza s paralelnim skupinama liječena su ukupno 234 ispitanika u dobi od 1 do 17 godina.
In a randomized, double-blind research study, patients with 40% overall body area burns were chosen to get common shed care plus oxandrolone, or without oxandrolone.
U randomiziranoj, dvostruko slijepoj studiji, osobe s 40% ukupne tjelesne površine opeklina su pokupili primati tipičan liječenju opekotina plus oxandrolone, ili bez oxandrolone.
The safety and efficacy of Respreeza was evaluated in a randomized, double-blind, placebo- controlled, multi-center study(RAPID) followed by a 2-year open-label extension study RAPID extension study.
Sigurnost i djelotvornost Respreeze procijenjena je u randomiziranom, dvostruko slijepom, placebom kontroliranom, multicentričnom ispitivanju(RAPID) nakon kojeg je slijedio 2-godišnji otvoreni nastavak ispitivanja nastavak RAPID ispitivanja.
In a randomized, double-blind research study, individuals with 40% complete body area burns were selected to get basic melt treatment plus oxandrolone, or without oxandrolone.
U randomiziranoj, dvostruko slijepoj studiji, osobe s 40% ukupno površine tijela opeklinama su pokupili dobiti osnovni tretman topljenju plus oxandrolone, ili bez oxandrolone.
Study 2(P02080) was a randomized, single centre study that enrolled 95 previously untreated adult patients with chronic hepatitis C who were co- infected with HIV.
Ispitivanje 2(P02080) bilo je randomizirano ispitivanje provedeno u jednom centru, u koje je uključeno 95 prethodno neliječenih odraslih bolesnika s kroničnim hepatitisom C koji su istodobno bili zaraženi HIV-om.
A randomized, double-blind, placebo--controlled study(Study 58) was conducted to demonstrate safety and efficacy of vandetanib 300 mg versus placebo.
Randomizirano, dvostruko slijepo, placebom kontrolirano ispitivanje(Ispitivanje 58) provedeno je s ciljem da se pokažu sigurnost primjene i djelotvornost vandetaniba u dozi od 300 mg u odnosu na placebo.
Study 02607 was a randomized, open-label, active-controlled, non-inferiority, multicenter clinical study in 159 patients previously stabilised with ERT.
Ispitivanje 02607 bilo je randomizirano, otvoreno, multicentrično kliničko ispitivanje neinferiornosti s aktivnom kontrolom na 159 bolesnika prethodno stabiliziranih s ERT-om.
A randomized, double-blind study was conducted to assess the safety and efficacy of abatacept or infliximab versus placebo in patients with an inadequate response to methotrexate Study V.
Provedeno je randomizirano, dvostruko slijepo ispitivanje sigurnosti i djelotvornosti abatacepta ili infliksimaba naspram placeba u bolesnika koji nisu dovoljno dobro odgovorili na metotreksat Ispitivanje V.
In a randomized, double-blind research study, patients with 40% total body area burns were selected to receive typical melt treatment plus oxandrolone, or without oxandrolone.
U randomiziranoj, dvostruko slijepoj studiji, osobe s 40% ukupne tjelesne površine opeklina su pokupili primati tipičan liječenju opekotina plus oxandrolone, ili bez oxandrolone.
In a randomized, double-blind study, patients with 40% complete body area burns were chosen to receive conventional burn care plus oxandrolone, or without oxandrolone.
U randomiziranoj, dvostruko slijepoj studiji, bolesnici s 40% ukupno površine tijela opeklinama, odabrani su za primanje konvencionalne brigu topljenju plus oxandrolone, ili bez oxandrolone.
In a randomized, double-blind research study, patients with 40% complete body area burns were selected to obtain common melt care plus oxandrolone, or without oxandrolone.
U randomiziranoj, dvostruko slijepoj studiji, bolesnici s 40% ukupno površine tijela opeklinama, odabrani su za primanje konvencionalne brigu topljenju plus oxandrolone, ili bez oxandrolone.
In a randomized, open-label study(SP825) in patients with early stage Parkinson's disease, 25 patients were randomized to rotigotine treatment and 26 to ropinirole.
U randomiziranom, otvorenom ispitivanju(SP825) u bolesnika u ranom stadiju Parkinsonove bolesti 25 bolesnika randomizirano je za liječenje rotigotinom, a njih 26 za liječenje ropinirolom.
In a randomized, double-blind research study, clients with 40% overall body surface area burns were chosen to get standard burn care plus oxandrolone, or without oxandrolone.
U randomiziranoj, dvostruko slijepoj studiji, bolesnici s 40% ukupno površine tijela opeklinama, odabrani su za primanje konvencionalne brigu topljenju plus oxandrolone, ili bez oxandrolone.
In a randomized, double-blind study, clients with 40% overall body surface area burns were selected to obtain standard shed treatment plus oxandrolone, or without oxandrolone.
U randomiziranoj, dvostruko slijepoj studiji, bolesnici s 40% ukupno površine tijela opeklinama, odabrani su za primanje konvencionalne brigu topljenju plus oxandrolone, ili bez oxandrolone.
In a randomized, double-blind research study, people with 40% complete body surface area burns were chosen to get common shed treatment plus oxandrolone, or without oxandrolone.
U randomiziranoj, dvostruko slijepoj studiji, bolesnici s 40% ukupno površine tijela opeklinama, odabrani su za primanje konvencionalne brigu topljenju plus oxandrolone, ili bez oxandrolone.
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