Pragmatic trials may deliver real world evidence on the added value of new medications compared to usual care and inform decision making earlier in development. This 5(th) paper in a series on pragmatic trials in the Journal discusses usual care as a comparator and the allocation of treatment strategies. The allocation and implementation of treatment strategies should resemble clinical practice as closely as possible. Randomization at the level of the site, as opposed to at the individual level, may be preferred. Data analysis according to the intention-to-treat principle is recommended, and crossover between treatment arms and strong treatment preferences may be accounted for in the study design in specific situations. Although usual care ...
Aim: Pragmatic clinical trials (PCTs) are randomized trials implemented through routine clinical pra...
Clinical research is a discipline prone to the use of technical terms that may be particularly at ri...
Background The CONSORT statement is intended to improve reporting of randomised controlled trials an...
Pragmatic trials may deliver real world evidence on the added value of new medications compared to u...
Results from pragmatic trials should reflect the comparative treatment effects encountered in patien...
This second article in the series on pragmatic trials describes the challenges in selection of sites...
This is the introductory paper in a series of eight papers. In this series, we integrate the theoret...
Results from pragmatic trials should reflect the comparative treatment effects encountered in patien...
Full list of author information is available at the end of the articleBackground Pragmatic and expla...
Abstract Introduction Pragmatic randomized controlled trials (RCTs) mimic usual clinical practice an...
Pragmatic trials can improve our understanding of how treatments will perform in routine practice. I...
Background Because pragmatic trials are performed to determine if an intervention can improve curren...
This paper addresses challenges of identifying, enrolling and retaining participants in a in a trial...
Aim: Pragmatic clinical trials (PCTs) are randomized trials implemented through routine clinical pra...
Clinical research is a discipline prone to the use of technical terms that may be particularly at ri...
Background The CONSORT statement is intended to improve reporting of randomised controlled trials an...
Pragmatic trials may deliver real world evidence on the added value of new medications compared to u...
Results from pragmatic trials should reflect the comparative treatment effects encountered in patien...
This second article in the series on pragmatic trials describes the challenges in selection of sites...
This is the introductory paper in a series of eight papers. In this series, we integrate the theoret...
Results from pragmatic trials should reflect the comparative treatment effects encountered in patien...
Full list of author information is available at the end of the articleBackground Pragmatic and expla...
Abstract Introduction Pragmatic randomized controlled trials (RCTs) mimic usual clinical practice an...
Pragmatic trials can improve our understanding of how treatments will perform in routine practice. I...
Background Because pragmatic trials are performed to determine if an intervention can improve curren...
This paper addresses challenges of identifying, enrolling and retaining participants in a in a trial...
Aim: Pragmatic clinical trials (PCTs) are randomized trials implemented through routine clinical pra...
Clinical research is a discipline prone to the use of technical terms that may be particularly at ri...
Background The CONSORT statement is intended to improve reporting of randomised controlled trials an...