Importance: Complete information in a trial protocol regarding study outcomes is crucial for obtaining regulatory approvals, ensuring standardized trial conduct, reducing research waste, and providing transparency of methods to facilitate trial replication, critical appraisal, accurate reporting and interpretation of trial results, and knowledge synthesis. However, recommendations on what outcome-specific information should be included are diverse and inconsistent. To improve reporting practices promoting transparent and reproducible outcome selection, assessment, and analysis, a need for specific and harmonized guidance as to what outcome-specific information should be addressed in clinical trial protocols exists. Objective: To develop har...
Patient reported outcomes (PROs) are used in clinical trials to provide valuable evidence on the imp...
Background: Clearly structured and comprehensive protocols are an essential component to ensure safe...
Abstract Background Clearly structured and comprehens...
Abstract Background Clinicians, patients, and policy-makers rely on published evidence from clinica...
Importance: Clinicians, patients, and policy makers rely on published results from clinical trials t...
Importance Patient-reported outcome (PRO) data from clinical trials can provide valuable evidence t...
Patient-reported outcomes (PROs) are used in clinical trials to provide valuable evidence on the imp...
Abstract Background Inadequate and poor quality outco...
Importance: Patient-reported outcome (PRO) data from clinical trials can provide valuable evidenc...
Background: Inadequate and poor quality outcome reporting in clinical trials is a well-documented pr...
Patient-reported outcomes (PROs) are used in clinical trials to provide valuable evidence on the imp...
Importance Trial protocols outline a trial’s objectives as well as the methods (design, conduct, an...
Contains fulltext : 237212.pdf (Publisher’s version ) (Open Access)BACKGROUND: Pro...
Patient-reported outcomes (PROs) are used in clinical trials to provide valuable evidence on the imp...
INTRODUCTION: Randomised controlled trials (RCTs) may use surrogate endpoints as substitutes and pre...
Patient reported outcomes (PROs) are used in clinical trials to provide valuable evidence on the imp...
Background: Clearly structured and comprehensive protocols are an essential component to ensure safe...
Abstract Background Clearly structured and comprehens...
Abstract Background Clinicians, patients, and policy-makers rely on published evidence from clinica...
Importance: Clinicians, patients, and policy makers rely on published results from clinical trials t...
Importance Patient-reported outcome (PRO) data from clinical trials can provide valuable evidence t...
Patient-reported outcomes (PROs) are used in clinical trials to provide valuable evidence on the imp...
Abstract Background Inadequate and poor quality outco...
Importance: Patient-reported outcome (PRO) data from clinical trials can provide valuable evidenc...
Background: Inadequate and poor quality outcome reporting in clinical trials is a well-documented pr...
Patient-reported outcomes (PROs) are used in clinical trials to provide valuable evidence on the imp...
Importance Trial protocols outline a trial’s objectives as well as the methods (design, conduct, an...
Contains fulltext : 237212.pdf (Publisher’s version ) (Open Access)BACKGROUND: Pro...
Patient-reported outcomes (PROs) are used in clinical trials to provide valuable evidence on the imp...
INTRODUCTION: Randomised controlled trials (RCTs) may use surrogate endpoints as substitutes and pre...
Patient reported outcomes (PROs) are used in clinical trials to provide valuable evidence on the imp...
Background: Clearly structured and comprehensive protocols are an essential component to ensure safe...
Abstract Background Clearly structured and comprehens...