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Eligibility criteria Double blind, randomised, controlled trials of acute treatment (six weeks or more) with reboxetine versus placebo or SSRIs in adults with major depression.
Eligibility Open label and double blind randomised controlled trials comparing one statin with another at any dose or with control (placebo, diet, or usual care) for adults with, or at risk of developing, cardiovascular disease.
As described previously, 14 15 16 17 we included open label and double blind randomised controlled trials comparing one statin with another at any dose or with control (placebo, diet, or usual care) for adults with, or at risk of developing, cardiovascular disease.
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The gold-standard test of medicine is the double blind, randomised controlled trial.
In the absence of country-specific studies, vaccine efficacy (VE) data for RIX4414 were collected from the double blind, randomised, controlled trial conducted in six European countries that was the basis for the approved Summary of Product Characteristics for Rotarix® [36, 37].
This study was a prospective, double blind, randomised controlled trial.
This is a prospective double blind randomised controlled trial which will be conducted at the University College London Hospital Endometriosis Centre.
The proposed study is a two-arm double blind randomised controlled trial.
We carried out a double blind randomised controlled trial over 12 months, the methodology of which has been described previously.
A double blind randomised controlled trial, assessing the effectiveness of the EBP training intervention, compared with a waitlist control, will be conducted.
The Alpha Tocopherol, Beta Carotene Cancer Prevention ATBCC) study was a double blind, randomised controlled trial to test α-tocopherol and β carotene among male smokers with no other previous serious illnesses.
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