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The information from this work may accelerate clinical trials and identify high-risk patients in need of preventative treatment.
Findings from these studies will provide indispensable tools for the design of future clinical trials and identify new perspectives and challenges for researchers and clinicians.
These data support risk stratification for future therapeutic trials and identify a predictor which needs to be validated in prospective studies and may potentially influence decision making in palliative management of patients with metastatic renal cell carcinoma.
These data support risk stratification for future therapeutic trials and identify factors that need to be validated in prospective studies and may potentially influence decision-making in palliative management of patients with disseminated cutaneous malignant melanoma.
Better and detailed understanding of physical activity undertaken during pregnancy and its correlates will inform the types and context within which physical activity might be promoted in randomized trials and identify the key confounding factors and nature of their associations with physical activity that need to be considered in observational epidemiology.
It would be advantageous to systematically review published RCTs that have carried out sub-group analyses, or those that have provided sufficient information to carry out sub-group analysis by pooling data from several trials and identify the most promising findings to date.
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We scanned the title and abstract of the trials identified to exclude those that were obviously irrelevant, retrieved the full text of the remaining trials, and identified relevant articles.
Inform the evidence base by describing how plans for PPI were implemented within clinical trials and identifying the challenges and lessons learnt by research teams.
Edwards' review on methods to increase response to postal and electronic questionnaires included 513 trials and identified many strategies to increase response to questionnaires (Edwards 2009).
We then screened a 1600-compound library of drugs that have been approved for use in human trials, and identified protective drugs (Fig. 1D).
In 2007 Al-Shahi Salman 6 retrospectively interviewed R&D departments from four trials and identified a median delay of 44 working days (IQR 23.0 80.0).
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com