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1 phase III, double-blind, placebo-controlled, multicentre trial.
2 randomised, placebo-controlled, double-blind multicentre trial.
3 ve, randomized, blinded, placebo controlled, multicentre trial.
4 lic hepatitis pending the results from large multicentre trials.
5 d, controlled, double-blind, parallel-group, multicentre trial (11 sites in Finland, Germany, the Net
6 rdised care can also facilitate planning for multicentre trials and help with the identification of a
8 We did a randomised, phase 2, open-label, multicentre trial at 37 centres in five countries and en
9 randomised double-blind, placebo-controlled, multicentre trial at three sites in Delhi (urban), Pune
12 ctive-controlled, open-label, international, multicentre trial, done at 106 sites across nine countri
17 2, randomised, parallel-group, double-blind multicentre trial in patients with New York Heart Associ
18 stic factors in this rare disease and assist multicentred trials in the evaluation of different treat
19 iated with poor functional outcomes; a large multicentre trial is currently comparing it against barb
20 adical prostate radiotherapy in the MRC RT01 multicentre trial (ISRCTN47772397, n=224) or in the Conv
21 In two placebo-controlled, double-blind, multicentre trials (M2-124 and M2-125) with identical de
26 ernational, open-label, randomised, phase 3, multicentre trial (TH CR-406/SARC021) at 81 academic or
28 ng cooperation and collaboration to complete multicentre trials that advance knowledge and patient ca
35 QUEST-1, a phase 3, randomised, double-blind multicentre trial undertaken in 13 countries (Australia,
37 ernational, open-label, randomised, phase 3, multicentre trial, we enrolled adult patients with CD30-
38 this pragmatic, randomised, parallel-group, multicentre trial, we recruited adults with symptoms sug
41 ion and treatment has improved, high-quality multicentre trials with long-term follow-up are needed.
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