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We performed a retrospective cohort study in which we enrolled TB patients who started DOTS treatment at Attapeu Provincial Hospital.
This was a cross sectional study in which we enrolled, consecutively, all consenting smear-positive newly diagnosed and retreatment TB patients aged ≥ 18 years.
This is a multicenter Italian prospective emergency department (ED) cohort study in which we enrolled 665 patients admitted to hospital from the ED.
After obtaining approval from Hospital das Clínicas ethics committee (approval number 1207/09), we conducted a prospective cohort study in which we enrolled 87 critically ill patients admitted to an ICU in a tertiary-care center in a large university hospital in São Paulo, Brazil, from February 2010 to January 2012.
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This nearly four-fold higher fall rate may be attributed to our differing participant inclusion criteria in which we only enrolled patients who had fallen during their hospital stay.
In this article, we report the rationale and study design for the ACS QUIK cluster-randomized stepped-wedge clinical trial (NCT02256657) in which we aim to enroll 15,750 participants with acute coronary syndromes across 63 hospitals.
Among them, we enrolled subjects which fulfilled the following inclusion criteria: age between 30 and 65 years, subjects meeting the American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) criteria for RA diagnosis [ 22], mean disease duration ≤ 24 weeks, BMI 16 25 kg/m, conscious acceptance of written informed consent.
We expect that the number of DD2 patients will increase substantially when the remaining GP clinics start enrolling patients, which we expect will happen within a short time.
We included studies which enrolled people with any disease type, receiving secondary care and we classified these as cancer and non-cancer.
We included studies which enrolled participants with the following factors: women who were postpartum, enrolled in the study in the early postpartum period (up to 12 weeks following delivery); women from any geographical and racial/ethnic background.
Thus, we excluded trials described as specifically targeting older people only, or which only enrolled people aged >65.
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