Exact(4)
About 90% of children in both study groups received one or more co-medications.
Both study groups received antibiotic treatment with either metronidazole or vancomycin.
As explained in the study information, participants in both study groups received written information on the complete study objectives and outcomes after termination of the study.
After the discharge, all patients from both study groups received the same daily exercise program, for duration of 18 days in a single rehabilitation center (Rehaklinik am Meer, Bad Zwischenahn, Germany).
Similar(56)
The risk of vertebral fracture was reduced 30%50%% in both study groups receiving raloxifene.
Both study groups receive free prescriptions for study medication, which is collected by the patients from local community pharmacies, and prescription data are captured on the electronic case report forms (eCRFs).
After the intervention period of 12 months, there will be a follow-up period of 6 months in which patients in both study groups receive TAU and no financial incentives for accepting their prescribed antipsychotic depot medication.
In the study of Lis, both control and study groups received premedication with misoprostol, diazepam, and pethidine.
In addition, while our study groups received a mixture and similar proportions of both non-leukoreduced and leukoreduced RBCs, the percentage of leukoreduced RBC units was not associated with survival on univariate or multivariate logistic regression analysis.
Study groups received similar sedative, opioid, and NMB dosing on days 1, 3, and 7. Patient comfort as assessed by clinicians was not different in the two groups: 93% perceived patients had no/minimal discomfort.
All three study groups received a copy of the British National Formulary (BNF) as a drug reference [ 6].
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