Examples of using Study entry in English and their translations into Swedish
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Ecclesiastic
-
Official/political
-
Computer
-
Programming
-
Political
At study entry, the mean HBV DNA was.
DNA negative and seronegative at study entry.
DNA- negativa och seronegativa vid studiestart.The age range at study entry was 1-6 months.
Åldersintervallet vid inskrivning i studien var 1-6 månader.The majority(75%) of patients had M1c stage disease at study entry.
Majoriteten(75%) hade stadium M1c vid studiestart.Of the 32 patients who had a liver biopsy at study entry, 100% had fibrosis and 31% had cirrhosis.
Av de 32 patienter som gjort en leverbiopsi vid inträdet i studien, hade 100% fibros och 31% hade cirros.
People also translate
or mutant(51%) at study entry.
eller mutant(51%) vid inklusion i studien.At study entry, the patients had an available deceased
Vid studiestart hade patienterna en tillgänglig avlidenA KRAS mutation was reported in 57% of patients at study entry.
KRAS-mutation rapporterades hos 57% av patienterna vid studiestart.At study entry patients were randomised to receive twice-daily doses of either 0.6 mg or 0.9 mg Signifor.
Vid studiestarten randomiserades patienterna till att få två dagliga doser av antingen 0, 6 mg eller 0, 9 mg Signifor.Sixty-one percent of patients had M1c stage disease at study entry.
Sextioen procent av patienterna hade M1c-melanom vid studiestart.IGF-I levels, which were low at study entry, were restored to within the normal range with somatropin therapy.
IGF-I-nivån, som var låg vid inträde i studien, återställdes till inom normalintervallet med somatropinbehandlingen.Patients had a median platelet count of 19 x 109/ l at study entry.
Patienterna hade ett mediantrombocytantal på 19 x 109/ l vid inträdet i studien.Detailed clinical status information will be collected at study entry and on an annual basis for at least 15 years.
Detaljerad information om klinisk status kommer att samlas in vid inträdet i studien och årligen 
However, only 65% of patients were receiving a PI based regimen at study entry.
Endast 65% av patienterna fick emellertid PI baserad behandling vid inträde i studien.In a subset defined as having less than 20 exposure days at study entry, less than 11% developed de-novo inhibitors.
I en undergrupp med kriteriet att ha haft mindre än 20 exponeringsdagar vid studiestart utvecklade färre än 11% de- novo inhibitorer.Efficacy against HPV-16/18 in women with evidence of HPV-16 or HPV-18 infection at study entry.
Effekt mot HPV 16/18 hos kvinnor med bevisad HPV 16- eller HPV 18-infektion vid studiestart.At study entry, 41% of randomized patients had PSA progression only,
Vid studiestart hade 41% av de randomiserade patienterna endast PSA-progression,58% had M1c disease at study entry.
58% hade M1c-sjukdom vid studiestart.At study entry, patients must have had penile curvature deformity of at least 30 degrees in the stable phase of Peyronie's disease.
Vid inskrivning i studien måste patienterna ha haft en penil kurvaturdeformitet på minst 30 grader Mean HbA1c increases were less pronounced in patients with normal glycaemia(n=62 overall) at study entry i.e.
Genomsnittliga HbA1c-ökningar var mindre uttalade hos patienter med normal glykemi(n=62 totalt) vid studiestart dvs.Approximately 45% of patients had measurable soft tissue disease at study entry, and 12% of patients had visceral(lung and/or liver) metastases.
Cirka 45% av patienterna hade mätbar mjukvävnadssjukdom vid studiestart och 12% av patienterna hade viscerala(lungor och/eller lever) metastaser.A majority of patients(67.2%) had not received disease-modifying therapy during the 2 years before study entry.
En majoritet av patienterna(67,2%) hade inte erhållit sjukdomsmodifierande behandling de närmaste 2 åren före inträdet i studien.Four of the five patients who required dialysis at study entry were able to discontinue dialysis for the duration of Soliris treatment, and one patient developed a new dialysis requirement.
Fyra av fem patienter som behövde dialys vid inträdet i studien kunde avbryta sin dialys under hela Solirisbehandlingen och en patient utvecklade nytt dialysbehov.36% of patients had a baseline LDH level greater than ULN at study entry.
36% av patienterna hade ett utgångsvärde för LDH högre än ULN vid studiestart.All patients received a 2-week standardised dose of prednisone 60 mg/day at study entry followed by a mandatory taper schedule,
Alla patienter fick en standardiserad 2-veckorsdos av prednison på 60 mg/dag vid studiestart följt av ett obligatoriskt nedtrappningsschema, med helt avbrutenas the primary diseases at study entry.
den primära sjukdomen vid studiestart.In the subgroup of 885 patients who were already receiving prophylactic heparin at study entry, mortality was 26.9% in the group randomised to continue heparin versus 35.6% in the group whose randomisation(to placebo) led to the discontinuation of heparin.
I den undergrupp på 885 patienter som redan erhöll heparin profylaktiskt vid studiestart var mortaliteten för den grupp som randomiserats till att fortsätta med heparin 26, 9% och för den grupp som randomiserats till placebo och där heparinadministrering avbröts 35, 6.were not in major cytogenetic response at time of study entry.
som inte visat betydande cytogenetiskt svar vid tiden för inträde i studien.At study entry, patients were treated with PAH medications(most frequently PDE-5 inhibitor[sildenafil]
Vid studiestart behandlades patienterna med PAH medicin(vanligast var ensam behandling med PDE-5 hämmare[sildenafil][35,9%],40 mg at study entry, and when experiencing a new attack thereafter.
229 patienter behandlades med triamcinolonacetonid(TA) 40 mg intramuskulärt vid studiestarten och därefter vid nya attacker.
