CONSORT extension for Traditional Chinese Medicine Formula 2017: recommendations, explanation and elaboration

CONSORT extension for Traditional Chinese Medicine Formula 2017: recommendations, explanation and elaboration

Chinese herbal medicine (CHM) formulas are the major components of traditional Chinese medicine (TCM) interventions. The general reporting quality of randomized clinical trials (RCTs) of CHM formulas is disappointing although there are CONSORT (Consolidated Standards of Reporting Trials) Statement e...

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Bibliografiske detaljer
Main Authors:	Cheng, C, Wu, T, Shang, H, Li, Y, Altman, D, Moher, D, Bian, Z, CONSORT-TCM Formula 2017 Group
Format:	Journal article
Udgivet:	American College of Physicians 2017

Lignende værker

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Extending the CONSORT statement to randomized trials of nonpharmacologic treatment; explanation and elaboration
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[CONSORT for reporting randomized controlled trials in journal and conference abstracts: explanation and elaboration].
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CONSORT 2010 explanation and elaboration: Updated guidelines for reporting parallel group randomised trials
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CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials.
af: Moher, D, et al.
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CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials.
af: Moher, D, et al.
Udgivet: (2010)

CONSORT 2010 Explanation and Elaboration: Updated guidelines for reporting parallel group randomised trials.
af: Moher, D, et al.
Udgivet: (2010)

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THE REVISED CONSORT STATEMENT FOR REPORTING RANDOMIZED TRIALS: EXPLANATION AND ELABORATION (2001)
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THE REVISED CONSORT STATEMENT FOR REPORTING RANDOMIZED TRIALS: EXPLANATION AND ELABORATION (2001) (ENDING)
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af: Schulz, K, et al.
Udgivet: (2010)

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af: Schulz, K, et al.
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CONSORT-SPI 2018 Explanation and Elaboration: guidance for reporting social and psychological intervention trials
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The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials.
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The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials.
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