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In order to avoid systematic reporting errors while ascertaining the high-quality reporting standards of RCTs, the CONSORT statement was coined in 1996.
The CONSORT diagram is a simple flow diagram showing the enrollment of subjects, their allocation to treatment, disposition status and how they are analysed in the trial. The layout of a CONSORT diagram depends on the study design.
The CONSORT Statement It offers a standard way for authors to prepare reports of trial findings, facilitating their complete and transparent reporting, and aiding their critical appraisal and interpretation.
Flow diagram of the progress through the phases of a parallel randomised trial of two groups (that is, enrolment, intervention allocation, follow-up, and data analysis).(52) (53) (54)
In order to avoid systematic reporting errors while ascertaining the high-quality reporting standards of RCTs, the CONSORT statement was coined in 1996.

People also ask

CONSORT is a protocol developed by a group of researchers not only to identify problems arising from conducting RCTs, but also to report, in a full and clear manner, the results yielded by research, thereby facilitating RCTs reading and quality assessment.
In addition to the checklist, CONSORT also encompasses a flow diagram which provides the reader with information about how the trial was conducted, reporting enrolment, allocation, follow-up and analysis of patients involved in the RCT (Fig 1).
The CONSORT (CONsolidated Standards of Reporting Trials) 2010 guideline is intended to improve the reporting of parallel-group randomized controlled trial (RCT), enabling readers to understand a trial's design, conduct, analysis and interpretation, and to assess the validity of its results.
A group of scientists and editors developed the CONSORT (Consolidated Standards of Reporting Trials) statement to improve the quality of reporting of RCTs. It was first published in 1996 and updated in 2001. The statement consists of a checklist and flow diagram that authors can use for reporting an RCT.
CONSORT stands for Consolidated Standards of Reporting Trials. Its main purpose is to improve the transparency and accuracy of reporting and interpreting the study results from a clinical trial.

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