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The intervention consists of up to 36 monthly educational modules delivered via telephone by a study pharmacist, home blood pressure monitoring, and medication management recommendations delivered electronically to primary care physicians.
Randomization envelopes were opened by a study pharmacist on the day of first immunization and immediately re-sealed after vaccine assignment.
Sequentially numbered bottles of either lidocaine or placebo will be arranged according to this schedule by a study pharmacist.
The study drug was prepared by a study pharmacist not involved in patient care and provided to the study physician in an infusion syringe labeled with the patient number and study identification.
Patient subjects are drawn from the medical and surgical inpatient, non-critical care units of each site, and are included if hospitalized long enough for a "gold-standard" medication history to be obtained by a study pharmacist (i.e., generally more than 24 hours).
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Randomization was conducted by the study pharmacist using a random number table and was revealed to study staff and investigators only at the conclusion of the study.
Women attended the clinic monthly to 24 weeks and at each visit VL was measured and an adherence assessment was done by the study pharmacist.
Randomization was performed by the study pharmacist, who prepared the vaccines and kept the study code.
The participants were enrolled by the clinical investigators and they were assigned to their treatment group by the study pharmacist on site (Djalakorodji, Mali).
with the escitalopram and placebo packed by the study pharmacist in sequentially numbered identical blister packs.
The treatment allocation scheme was maintained by the study pharmacist who assumed the responsibility for blinded drug distribution.
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