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This study describes the registry design, data collection, outcomes validation, and ongoing surveillance, highlighting the unique integration with the EMR.
The OUCH-PRO Study is a prospective multicenter single-arm registry design to study clinical and angiographic outcomes after everolimus-eluting stent (EES).
The longitudinal registry design resembles a "real world" setting without the typical clinical trial selection bias.
Details of the CONFIRM registry design and data elements have been published.
This analysis has a number of limitations related to the Gaucher Registry design and study exclusion criteria.
Limitations of our study are the non-randomised and monocentric registry design without control group concerning ischaemic events.
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Patients enrolled into a treatment registry designed to track patient safety and treatment outcomes.
REACH is the largest international registry designed to identify the clinical characteristics of atherothrombosis in the real-life setting.
The article presents a population-based registry designed to estimate incidence and prevalence of inflammatory bowel disease (IBD) in the area of Forlì (north-eastern Italy).
The Stent Comparative Restenosis (SCORES) Saphenous Vein Graft (SVG) Registry was a multicenter, prospective registry designed to evaluate the safety and efficacy of a self-expanding, nickel-titanium (nitinol) stent for de novo SVG lesions.
The REACH Registry is the largest worldwide registry designed to obtain information on cardiovascular risk factor control and preventive treatment in a population who have, or are at high risk of having, symptoms of atherothrombosis.
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CEO of Professional Science Editing for Scientists @ prosciediting.com