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The present study has been designed to trial fluorescence lymphangiography for establishing how lymphatic function is altered under a clinically relevant form of mechanical loading.
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This study was designed to trial the methodology as the first phase of a larger program of work.
A controlled trial was designed to test the effectiveness of the Heart Health Counts (HHC) program.
The trials were designed to test the efficacy of various drug combinations in differing doses.
This trial has been designed to complement two other clinical trials: B-Unaware[ 15] (NCT00281489) and MACS (NCT00689091).
The concept of clinical trial registry has been designed to disseminate knowledge about clinical trials.
Therefore, the trial was designed to be largely a pragmatic trial.
This trial is designed to be a feasible, comparative effectiveness trial design that is similar to common clinical situations.
14 The trial was designed to assess equivalence between the two trial arms in the primary clinical outcome.
Superiority trials are designed to detect larger differences than noninferiority trials are designed to rule out.
The RE-MEDY trial was designed as a non-inferiority trial, while the RE-SONATE trial was designed to demonstrate superiority of dabigatran [ 30].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com