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Clients provided information for 454 (75.9%) of the children that had been evaluated at baseline.
Efficacy parameters have been evaluated at baseline and after 15 weeks by blinded-observers.
A total of 116 participants have been evaluated at baseline, 90 participants have been evaluated immediately after treatment (6-week follow-up after randomization) and 30 participants have been assessed at the 6-month follow-up after randomization.
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Outcomes were evaluated at baseline, 3-month, and 6-month follow-ups.
Metabolic markers were evaluated at baseline and at the end of the study.
Participants were evaluated at baseline and at 6-month intervals with standardized interview instruments.
Antibody levels to 11 Pn strains were evaluated at baseline and 1-month.
Clinical and neurohumoral status were evaluated at baseline, on chronic therapy at the target dose, and during cessation of therapy.
Fasting lipoprotein and lipid measurements were evaluated at baseline and at 8-week intervals during the Reference and MUFA diets.
Main Outcome Measures: Outcome measures were evaluated at baseline and at 1, 2, 3, and 6 months.
Menstrual pain, physical fitness, and QOL were evaluated at baseline and at the end of the 12-week study period.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com