您搜索了: topeltpimeuuringus (爱沙尼亚语 - 英语)

trudexa efektiivsust ja ohutust reumatoidartriidi ravis uuriti viies randomiseeritud ja kontrollitud topeltpimeuuringus.
the efficacy and safety of trudexa for the treatment of rheumatoid arthritis were assessed in five randomised, double-blind and well-controlled studies.

kliinilises topeltpimeuuringus randomiseeriti 2927 patsienti saama fondapariinuksit 2, 5 mg üks kord päevas või daltepariini 5000 rÜ
in a double-blind clinical study, 2927 patients were randomized to receive fondaparinux 2.5mg once daily or dalteparin 5000 iu once daily, with one 2500 iu preoperative injection and a first 2500 iu m

pp prospektiivses randomiseeritud platseebokontrolliga topeltpimeuuringus 344 lümfoproliferatiivse pahaloomulise kasvajaga aneemilise patsiendiga, kes said keemiaravi, vähenes oluliselt
in patients not on dialysis, once the target haemoglobin has been achieved with once every two week lo dosing, nespo may be administered subcutaneously once monthly using an initial dose equal to twice the previous once every two week dose. no

26-nädalases topeltpimeuuringus võrreldi toimeainet prolongeeritult vabastavat eksenatiidi sitagliptiini ja pioglitasooni maksimaalsete päevaste annustega uuritavatel, kes kasutasid ka metformiini.
in a 26-week double-blind study prolonged-release exenatide was compared to maximum daily doses of sitagliptin and pioglitazone in subjects also using metformin.

suures topeltpimeuuringus oli suukaudse kolmikravi kasutamisel südamepuudulikkuse esinemissagedus 1,4% võrreldes 0,4%-ga metformiini pluss sulfonüüluurea kaksikravi puhul.
the incidence of heart failure on triple oral therapy was 1.4% in the main double blind study, compared to 0.4% for metformin plus sulphonylurea dual therapy.

laste (4...16-aastastel) tõestati levetiratsetaami efektiivsus platseebokontrollitud topeltpimeuuringus, mis hõlmas 198 patsienti ravi kestusega 14 nädalat.
in paediatric patients (4 to 16 years of age), levetiracetam efficacy was established in a double-blind, placebo-controlled study, which included 198 patients and had a treatment duration of 14 weeks.

levetiratsetaami efektiivsust uuriti 16 nädalat kestnud platseebo-kontrolliga topeltpimeuuringus, kus osalesid üle 12-aastased patsiendid idiopaatilise generaliseerunud epilepsiaga ja müoklooniliste krampidega erinevate sündroomide korral.
levetiracetam efficacy was established in a double-blind, placebo-controlled study of 16 weeks duration, in patients 12 years of age and older suffering from idiopathic generalized epilepsy with myoclonic seizures in different syndromes.

cholestagel’i 3,8 g päevase annuse lisamist statiini ja esetimiibi kombinatsioonravile maksimaalselt talutavas annuses hinnati mitmekeskuselises, randomiseeritud, platseebokontrolliga topeltpimeuuringus, mis hõlmas 86 patsienti perekondlikku hüperkolesteroleemiaga.
the addition of cholestagel 3.8 g daily to maximally-tolerated statin and ezetimibe therapy was assessed in a multi-centre, randomised, double-blind, placebo-controlled study in 86 patients with familial hypercholesterolaemia.

9 Ühes topeltpimeuuringus võrreldi tasmar’ it entakapooniga parkinsoni tõvega patsientidel, kellel esines optimaalse levodopa- ravi ajal vähemalt 3- tunnine off- aeg päevas.
a double-blind trial compared tasmar with entacapone in parkinson's disease patients who had at least three hours of off time per day while receiving optimised levodopa therapy.

prospektiivses randomiseeritud platseebokontrolliga topeltpimeuuringus, milles osales 314 kopsuvähiga patsienti, kellele manustati plaatinat sisaldavat keemiaravi, vähenes oluliselt vereülekannete vajadus (p < 0,001).
in a prospective, randomised double-blind, placebo-controlled study conducted in 314 lung cancer patients receiving platinum containing chemotherapy there was a significant reduction in transfusion requirements (p < 0.001).