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studiedesign
study design
Last Update: 2017-04-26
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studiedesign (region)
study design (region)
Last Update: 2017-04-26
Usage Frequency: 1
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resumé af studiedesign
summary of study design
Last Update: 2017-04-26
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tabel 2: studiedesign
table 2: study design
Last Update: 2017-04-26
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studiedesign og baseline-karakteristika er vist i tabel 3.
the study designs and baseline characteristics are presented in table 3.
Last Update: 2017-04-26
Usage Frequency: 1
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tabel 2: studiedesign og baseline-karakteristika for studie 1 og 2
table 2: study design and baseline characteristics for studies 1 and 2
Last Update: 2017-04-26
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studiedesign/demografi og resultater for studie 1 og 2 fremgår af henholdsvis tabel 2 og 3.
for studies 1 and 2, study design/demographics and results are shown in table 2 and table 3 respectively.
Last Update: 2017-04-26
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tabel 11: studier udført med simeprevir + sofosbuvir: population og resumé af studiedesign
table 11: studies conducted with simeprevir + sofosbuvir: population and summary of study design
Last Update: 2017-04-26
Usage Frequency: 1
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det overordnede studiedesign var identisk i begge stadier, og patienterne blev randomiseret til en af følgende to behandlingsgrupper:
the overall trial design was identical among both stages and patients were randomized into the following two treatment groups:
Last Update: 2017-04-26
Usage Frequency: 1
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tabel 3: studiedesign og baseline-karakteristika for select-studiet og decide-studiet
table 3: study design and baseline characteristics for select study and decide study
Last Update: 2017-04-26
Usage Frequency: 1
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i henhold til studiedesign kan patienterne i langtids- opfølgningsperioden have skiftet mellem doserne 50 mg og 100 mg simponi efter studielægens skøn.
by study design, patients in the long-term extension may have switched between the 50 mg and 100 mg simponi doses at the discretion of the study physician.
Last Update: 2017-04-26
Usage Frequency: 1
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som det var forventet på basis af studiedesignet, sås ingen forskel i varighed af remission, sygdomsfri overlevelse eller generel overlevelse, skønt patienter med komplet molekylær respons og forblivende i minimal residual sygdom havde større udbytte af behandlingen i form af både varighed af remission (p = 0,01) og sygdomsfri overlevelse (p = 0,02).
as expected on the basis of the study design, no difference was observed in remission duration, disease-free survival or overall survival, although patients with complete molecular response and remaining in minimal residual disease had a better outcome in terms of both remission duration (p = 0.01) and disease-free survival (p = 0.02).
Last Update: 2017-04-26
Usage Frequency: 8
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