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In his report last year, which was commissioned by the Lord Chief Justice, Lord Leveson said: "Our conduct of criminal trials was designed in the 19th century with many changes and reforms bolted on, especially over the last 30 years.
This meta-analysis of patient data from 26 randomised controlled trials was designed to assess safety of procalcitonin-guided treatment in patients with acute respiratory infections from different clinical settings.
Formal approval for general clinical use, however, required that systematic data be gathered on buprenorphine's safety and efficacy in larger groups and a series of controlled clinical trials was designed to evaluate its utility from a medication development perspective.
This set of trials was designed to include all eight major forest growing regions.
An appropriate set of trials was designed to investigate the possibility of not simulating accurately the radiographic process.
One of the trials was designed to transplant alginate encapsulated human islets intraperitoneally, and the other one was to explore potential implantation sites (i.e. peritoneum, omentum, and brachioradialis muscles), for encapsulated islet transplantation.
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The trials were designed to test the efficacy of various drug combinations in differing doses.
Most trials are designed around the information drug regulators require to license a new treatment.
All existing clinical trials were designed using this strategy.
And they are demanding — and receiving — more of a say in how clinical trials are designed and conducted.
The device, currently in clinical trials, is designed to quickly predict if patients will respond to an antidepressant.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com