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Results and Outcome Reporting In ClinicalTrials.gov, What Makes it Happen?

Overview of attention for article published in PLOS ONE, June 2012
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Title
Results and Outcome Reporting In ClinicalTrials.gov, What Makes it Happen?
Published in
PLOS ONE, June 2012
DOI 10.1371/journal.pone.0037847
Pubmed ID
Authors

Olga Kirillova

Abstract

At the end of the past century there were multiple concerns regarding lack of transparency in the conduct of clinical trials as well as some ethical and scientific issues affecting the trials' design and reporting. In 2000 ClinicalTrials.gov data repository was developed and deployed to serve public and scientific communities with valid data on clinical trials. Later in order to increase deposited data completeness and transparency of medical research a set of restrains had been imposed making the results deposition compulsory for multiple cases.

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The data shown below were collected from the profiles of 3 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 30 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 7%
Unknown 28 93%

Demographic breakdown

Readers by professional status Count As %
Student > Master 8 27%
Student > Ph. D. Student 6 20%
Researcher 4 13%
Librarian 3 10%
Student > Doctoral Student 2 7%
Other 4 13%
Unknown 3 10%
Readers by discipline Count As %
Medicine and Dentistry 8 27%
Agricultural and Biological Sciences 5 17%
Economics, Econometrics and Finance 3 10%
Social Sciences 3 10%
Nursing and Health Professions 1 3%
Other 6 20%
Unknown 4 13%