Voorbeelden van het gebruik van Secondary endpoint in het Engels en hun vertalingen in het Nederlands
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Overall Survival- secondary endpoint.
A key secondary endpoint is the restoration of haemostasis.
Overall survival(OS) was the key secondary endpoint.
Efficacy was a secondary endpoint in this study.
Exercise capacity was evaluated as a secondary endpoint.
Mensen vertalen ook
The secondary endpoint of Overall Survival(OS)
Percentage Change in Liver Volume MN(%) secondary endpoint.
The 144 week secondary endpoint data are also presented in Table 1.
Percentage Change in Platelet Count(%) secondary endpoint.
Also the first secondary endpoint(all cause death,
Absolute Change in Haemoglobin Level(g/dL) secondary endpoint.
Fistula healing was studied as a secondary endpoint in the Humira maintenance trial.
OS was the key secondary endpoint.
A key secondary endpoint was the continuous abstinence(CA)
In the RUTH study overall clinical fractures were collected as a secondary endpoint.
The main secondary endpoint was MCyR by total daily dose level in the imatinib-resistant patients.
in CP patients was evaluated as a secondary endpoint.
The secondary endpoint was complete remission rate that was assessed by independent expert review.
stroke were assessed as secondary endpoint.
A key secondary endpoint was the incidence of proven/probable IFIs at 100 days post-randomization.
hospitalisation for PAH was assessed as a secondary endpoint.
The major secondary endpoint was the proportion of patients who achieved a sPGA score of clear(0)
Efficacy of Prevenar against AOM was assessed as a secondary endpoint in the Kaiser Permanente trial.
In study MenACWY-TT-104, serum bactericidal activity was also measured using hSBA as a secondary endpoint.
Additionally, lurasidone was superior to placebo on the predefined secondary endpoint Clinical Global Impression- Severity(CGI-S) scale.
Adjusted mean change from baseline in trough FEV1 was also evaluated as a secondary endpoint.
A key secondary endpoint was the incidence of proven/ probable IFIs during the on-treatment period first dose to last dose of study medicinal product+ 7 days.
The primary endpoint of the study was overall survival with a key secondary endpoint of PFS.
The primary endpoint was time to disease progression and the secondary endpoint was overall survival.
Change from baseline in the percentage of rescue-free 24 hour periods during treatment was a powered secondary endpoint.