Trends in Data Monitoring Committees, Randomization, and Blinding in Cardiovascular Disease Studies on ClinicalTrials.gov from 2012 to 2021

Author:

Rawlley BharatORCID,Bansal Kannu,Dayal Utkarsh,Julka Dhawani,Salooja Ishita,Sanchez Andres Cordova,Gupta Kartik,Kumar Sandeep,Chaudhuri DebanikORCID

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference5 articles.

1. The quality of registration of clinical trials;Viergever;PLoS One,2011

2. U.S. Food and Drug Administration. Establishment and operation of clinical trial Data Monitoring Committees. Available at: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/establishment-and-operation-clinical-trial-data-monitoring-committees. Accessed on April 1, 2023.

3. Characteristics of clinical trials registered in ClinicalTrials.gov, 2007–2010;Califf;JAMA,2012

4. Effect of characteristics of women on attendance in blind and non-blind randomised trials: analysis of recruitment data from the EPHT trial;Veerus;BMJ Open,2016

5. Characteristics of clinical trial websites: information distribution between ClinicalTrials.gov and 13 primary registries in the WHO registry network;Ogino;Trials,2014

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