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A prospective, randomized, controlled study was designed; eligible patients were randomly assigned to pharmaceutical intervention (PI) group and control group by random number table.
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Study design: Eligible infants (n = 131) <2 years of age requiring open heart surgery were recruited prospectively.
Study Design: Eligible participants included women aged 25to6969 years who complained of persistent uterine bleeding, despite medical treatment.
Study design: Eligible infants were enrolled after surgery when serum direct bilirubin (DB) was <2 mg/dL.
Methods By a 2 × 2 × 2 factorial design, eligible participants (N = 468) were randomly assigned to low-dose warfarin, antioxidant vitamins, and niacin or its corresponding placebo, and followed up for 1 year.
Study design: Eligible for the study were 4228 women aged 18 70 years with symptomatic low gynecological tract infection and clinical findings suggestive for Candida infection consecutively attending during the study period first level outpatients gynecological services in Italy.
Study designs eligible for inclusion were randomised controlled trials, interrupted time series and controlled before-after studies that assessed the impact of personal security alarms on assaults.
EXPERIMENTAL DESIGN: Eligible patients with tumors accessible for core needle biopsy were treated with SU6668 at doses of 200 or 400 mg/m(2)/day.
In quantitative reviews, criteria are generally narrow [ 4], with only certain study designs eligible for inclusion e.g. randomised controlled trials.
Study designs eligible for this review were systematic reviews, randomized controlled trials (RCT), quasi-randomized controlled trials, controlled before-after studies and interrupted time series.
Using a parallel design, eligible children with parental consent were randomized to the intervention and control groups with a 1 1 allocation ratio.
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CEO of Professional Science Editing for Scientists @ prosciediting.com