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Patients with antihypertensive medication were instructed to continue treatment.
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Eligible patients received 2 bottles of appropriate study medication and were instructed to administer the medication to the study eye once daily at 8 pm for 6 weeks.
They were asked to report if they became ill or required medications and were instructed not to donate semen samples during those times.
As with SAT participants, DAART participants took home an EAM device for their monitored medication and they were instructed to take medication from the EAM device whenever they took a "home" dose (e.g., evening or weekend doses).
For compliance, patients were asked directly if they were taking their medication as they were instructed.
All participants were medication free and were instructed not to use any substance of abuse, including coffee, on the day of the scan.
One week after the last injection with the trial medication the participants were instructed to return to their own general practitioner for assessment of short-term outcomes.
Two weeks after the injections with the trial medication the participants were instructed to return to their own general practitioner for assessment of short-term outcomes.
Women who consumed the medication at home were instructed to bring the empty blister packets with them to the health facility during their postpartum visit and newborn's first immunization visit.
FM patients that used analgesics and/or sleep medicine on a regular basis were instructed to cease medication two days prior to the experiment.
All subjects took their medication at the usual time and were instructed not to perform any extra physical activity on testing days.
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