Sentence examples for weeks were randomized from inspiring English sources

Women who were between the gestational ages of 10 and 18 weeks were randomized from three clinical centers across the United States — Boston Medical Center, Washington University in St . Louis and Kaiser Permanente Southern California Region (San Diego, CA).

Eligible patients with OIC (n = 207), defined as <3 spontaneous bowel movements (SBMs) per week with accompanying symptoms, on a stable opioid regimen of 30 1000 mg/day morphine equivalents for ⩾2 weeks were randomized to receive 4 weeks of double-blind placebo or naloxegol (5, 25, or 50 mg) once daily in sequential cohorts after a 1-week placebo run-in.

Study Design: In this double-masked, controlled clinical trial, pregnant women with diabetes and gestational age of >38½ weeks were randomized to receive 25 μg misoprostol or placebo vaginally on days 1 and 4 of a 7-day outpatient cervical ripening period.

Study Design: One hundred fifty-seven pregnant women with a singleton live gestation, Bishop score of <7, estimated fetal weight of <4500 g, and gestational age of >24 weeks were randomized to receive misoprostol that would be placed either in the buccal pouch or vagina every 6 hours.

Patients with stable disease at 12 weeks were randomized to either continue pazopanib or a placebo.

Male C57BL/6 J mice, age 8 12 weeks, were randomized into four groups: vehicle, DDFPe, 5-HD + vehicle, and 5-HD + DDFPe.

Workers still on sick leave at 8 weeks are randomized for the Graded Activity intervention.

Adults with opioid-induced constipation (OIC; <3 spontaneous bowel movements [SBMs] per week) were randomized 1 1 to double-blind lubiprostone 24 μg or placebo twice daily for 12 weeks.

Heimstad conducted a trial where women in the 41st gestational week were randomized to a waiting group or an induction group and asked about their attitudes towards post-term pregnancy [ 7].

Adult participants (n = 400) with LE OA, age 60 +, overweight/obese, and not meeting PA requirements of  ≥ 150 min per week, are randomized to one of the two programs.

After 2 weeks, subjects were randomized to 2 additional weeks of concomitant budesonide aqueous nasal spray (n = 9) or placebo (n = 10).