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OS was calculated as the time from date of entry in the trial until date of death from any cause.
Participants were required to have a habitual sleep onset time before 1 A.M., and a habitual sleep end time before 9 A.M., prior to entry in the trial.
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TB screening prior to entry in the trials may have resulted in a lower incidence of TB in the abatacept CDP.
Malignancy screening for breast cancer with mammograms before entry in the trials may have resulted in a lower incidence of breast cancer in the abatacept CDP.
Whereas in a randomized controlled trial the randomization occurs at entry into the trial, in MR the randomization occurs during gamete formation and conception.
Baseline demographic and clinical characteristics for all intervention groups at entry into the trial are shown in Table 1.
At entry into the trial, sexually active women in this ancillary study had significant impairments across all major domains of sexual function compared with normative controls (14).
The control patients showed no change in MRI from baseline at entry into the trial.
Previous entry in the present trial.
This was the same definition used to exclude patients from entry in the parent trial owing to uncontrolled baseline hypertension.
Survival times were calculated from the date of entry in the BFR14 trial (i.e. initiation of IM treatment) and were displayed using the Kaplan-Meier method [ 18].
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