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A protocol summary of a randomised controlled trial.
Protocol Summary: Participants will have up to four visits.
Protocol Summary: A total of 100 HIV+ patients from the Duke HIV clinic will be enrolled.
Protocol Summary: The study consists of participating in a one on one interview with a study coordinator lasting approximately 30 minutes.
Protocol Summary: A sample of 30 HIV-infected cancer patients from the Duke HIV clinic and Duke Cancer Institute Clinics will be interviewed one-on-one to identify the themes associated with barriers to receiving adequate cancer treatment.
Protocol Summary: This is a Phase 2 open label PK, safety, and antiviral activity of GS-9883/Emtricibine GS-9883/Emtricibinenamide (TAF /Tenofovire combinAlafenamideV-1 infecTAF virologically suppressed adolescents and children.
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The useful protocol summaries of Swindles et al. [29], Turney [60], and Blockley and colleagues [61] lay out the guidelines for these complementary methods.
Currently, brief protocol summaries, including aims, primary outcomes, inclusion and exclusion criteria, duration of the trial, and planned intervention, of all clinical trials are available on the internet.
ICMJE in 2004 [ 12], the Declaration of Helsinki revised in 2008 [ 17] and the CONSORT declaration in 2010 [ 18] request the disclosure of trial protocol summaries and results by sponsors of clinical trials to avoid publication biases.
Information that parties are required to provide to the Clearing-House includes existing laws, regulations and guidelines for implementation of the Protocol; information required for the AIA; any bilateral, regional and multilateral agreements within the context of the Protocol; summaries of risk assessment and final decisions.
As the single point of access to all registered clinical trials, it is important that the ICTRP database is searchable for individual records, that it provides opportunity for aggregate analyses, and that it links to the related trial documents and data mentioned in the previous section (protocols, summary results, clinical study reports, publications and participant-level data).
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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