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More than half (54.5%) of the patients who participated in Trial 208 were able to resume treatment with delamanid within 2 months of completing Trial 204; however, more than one-third resumed treatment after ≥4 months.
Thirdly, as Study 116 was initiated close to the completion of Trial 204, with retrospective capture of data for some patients completing Trial 204 earlier in its conduct, information bias may have been introduced.
T = 3: The visit at month 12 15 after randomisation is focused on completing trial participation.
The 3-month lag was due to technical difficulties in completing trial registration.
Our subjects were exposed to nCPAP for a 7-day adaptation period prior to completing Trial 2. This adaptation period occurred after a baseline study was completed.
These have included patients obtaining beneficial effects from helping others through participating in research [ 29], and insights gained through completing trial diaries of their symptoms [ 16].
Similar(49)
MADDERS can also be applied retrospectively to completed trial data.
Conclusion: Data from the completed trial will be presented at the meeting.
Analysis was completed before the randomisation code was broken at the end of the completed trial.
That is, after trial 1 of KSF was completed, trial 1 of KSB was administered.
††All reported data refer to women who completed trial; 108 and 99 women were recruited.
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