Examples of using To study entry in English and their translations into Swedish
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Each patient had to have at least 90 seizures in the month prior to study entry.
Among patients who had received imatinib 400 mg prior to study entry, MCyR was achieved in 61% of patients in the dasatinib arm and 50% in the imatinib arm.
Hos patienter som hade behandlats med imatinib 400 mg före studiestart uppnåddes MCyR hos 61% av patienterna i dasatinib-armen och hos 50% av patienterna i imatinib- armen.Each patient had to have at least 90 seizures in the month prior to study entry.
Recent surgery(within 30 days prior to study entry) was associated with a numerically higher risk of serious bleeding during infusion in both the Xigris-treated
Nyligen genomgången operation(under de senaste 30 dagarna före studiestart) var förenat med en numeriskt högre risk för allvarlig blödning under infusionen hostreatments for ITP prior to study entry.
behandlingar för ITP före inträdet i studien.Patients had to be stably suppressed for at least 8 weeks prior to study entry, have no current
Patienterna måste ha varit stabilt hämmade The median cumulative RAI activity administered prior to study entry was 350 mCi 12.95 GBq.
Medianvärdet för kumulativ RAI-aktivitet administrerat före inträde i studien var 350 mCi 12, 95 GBq.In Studies I and II only, patients were required to have at least one asthma exacerbation requiring systemic corticosteroid use in the year prior to study entry.
Endast i studie I och II måste patienterna ha haft minst en astmaexacerbation som krävde användning av systemisk kortikosteroid under året före studiestart.baseline performance score≥ 2, active brain metastases or autoimmune disease, and patients who had been receiving systemic immunosuppressants prior to study entry were excluded from the clinical trials of nivolumab or nivolumab in combination with ipilimumab.
aktiva hjärnmetastaser eller autoimmun sjukdom samt patienter som hade fått systemisk immunsuppressiv behandling före studiestart, exkluderades i kliniska studier med nivolumab eller nivolumab An analysis showed that serious adverse events were reported in 39.4% of those patients who switched from agalsidase beta compared to 31.0% in those who were naïve to therapy prior to study entry.
En analys visade att allvarliga biverkningar rapporterades hos 39, 4% av de patienter som bytte från agalsidas beta jämfört med 31, 0% av dem som var naiva för behandling före studiestart.Recent surgery(within 30 days prior to study entry) was associated with a numerically higher risk of serious bleeding during infusion in both the Xigris-treated
Nyligen genomgången operation(under de senaste 30 dagarna före studiestart) var förenat med en numeriskt högre risk för allvarlig blödning under infusionen hosThe average number of gout flares per patient was 10 during the 18 months prior to study entry.
Varje patient hade The safety and efficacy of romiplostim was evaluated in two placebo-controlled, double-blind studies in adults with ITP who had completed at least one treatment prior to study entry and are representative of the entire spectrum of such ITP patients.
Säkerheten och effekten för romiplostim utvärderades patients who had been receiving systemic immunosuppressants prior to study entry were excluded from the clinical trials of NSCLC see sections 4.5 and 5.1.
symtomatisk interstitiell lungsjukdom och patienter som hade fått systemisk immunsuppressiv behandling före studiestart, exkluderades från kliniska studier på icke-småcellig lungcancer se avsnitt 4.5 och 5.1.older who were naïve to ERT defined as having not been treated with ERT for at least 30 months prior to study entry.
dubbelblind effektstudie med parallella grupper på 25 patienter who had reported a total of 15 crises in the 12 months prior to study entry while they were being treated with sodium phenylbutyrate.
totalt 10 hyperammonemiska kriser under behandling med glycerolfenylbutyrat, jämfört med 9 patienter(18%) som hade rapporterat totalt 15 kriser under de 12 månaderna före inskrivning i studien medan de behandlades med natriumfenylbutyrat.documented radiographic disease progression within 14 months prior to study entry.
metastaserande MTC och dokumenterad radiologisk sjukdomsprogression inom 14 månader före inträdet i studien.in the preceding 12 months prior to study entry, while they were being treated with sodium phenylbutyrate.
under behandling med glycerolfenylbutyrat, jämfört med 38 kriser hos 21 patienter(43%) under de 12 månaderna före inskrivning i studien, medan de behandlades med natriumfenylbutyrat.22 GBq with the last dose at least 6 months prior to study entry.
aktivitet av RAI på> 600 mCi eller 22 GBq med den sista dosen minst sex månader före inträde i studien.Adjuvant taxane therapy was allowed only if it was completed at least 12 months prior to study entry.
Adjuvant taxanbehandling var tillåtet endast om den hade avslutats minst 12 månader innan studieinklusion.One hundred and twelve(89.6%) subjects were refractory to their last regimen prior to study entry.
Etthundratolv(89, 6%) patienter var refraktära mot den senaste regimen före registrering i studien.treatments for ITP prior to study entry.
behandlingar för ITP före inträdet i studien.older who were naïve to ERT defined as having not been treated with ERT for at least 12 months prior to study entry.
kontrollerad,”non-inferiority”- effektstudie med aktiv komparator(imiglukeras) och parallella grupper med 34 patienter Death or disability according to subgroup of respiratory support at entry to study.
Död eller invaliditet efter undergrupp av andningsstöd vid inträdet i studien.
