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Large randomized controlled trials in infertility.
Wang, Rui; Chen, Zi-Jiang; Vuong, Lan N; Legro, Richard S; Mol, Ben W; Wilkinson, Jack.
Afiliação
  • Wang R; Department of Obstetrics and Gynaecology, Monash University, Clayton, Australia. Electronic address: r.wang@monash.edu.
  • Chen ZJ; Center for Reproductive Medicine, Shandong University, Jinan, Shandong; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Shandong University, Jinan, Shandong; Shandong Provincial Clinical Medicine Research Center for Reproductive Health, Shandong University, J
  • Vuong LN; Department of Obstetrics and Gynecology, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam.
  • Legro RS; Department of Obstetrics and Gynecology, Penn State College of Medicine, Hershey, Pennsylvania.
  • Mol BW; Department of Obstetrics and Gynaecology, Monash University, Clayton, Australia.
  • Wilkinson J; Centre for Biostatistics, University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom.
Fertil Steril ; 113(6): 1093-1099, 2020 06.
Article em En | MEDLINE | ID: mdl-32482244
ABSTRACT
As the first paper in this series of Views and Reviews on randomized controlled trials (RCTs), we aim to provide the basics of RCTs in infertility research. In this paper, we discuss the need and ethical considerations of large trials in infertility research and important aspects to guarantee the quality of a trial, including protocols, registrations and monitoring, issues of study design and analysis, and reporting standards. Because most of the treatment effects we would like to study represent relatively small signal-to-noise ratios, large RCTs are required to provide sufficient power to answer these questions. Trial protocols, registrations, and monitoring facilitate the transparency of conduct, analysis, and reporting of the trial. Issues of trial design and analysis, such as nonblinding and misuse of the denominators, are common in published trials in this area and could be further improved. Finally, following the current reporting standard facilitates complete and transparent reporting, critical appraisal, and interpretation.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Controlados Aleatórios como Assunto / Medicina Reprodutiva / Medicina Baseada em Evidências / Infertilidade Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline Aspecto: Ethics Limite: Female / Humans / Male Idioma: En Revista: Fertil Steril Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Controlados Aleatórios como Assunto / Medicina Reprodutiva / Medicina Baseada em Evidências / Infertilidade Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline Aspecto: Ethics Limite: Female / Humans / Male Idioma: En Revista: Fertil Steril Ano de publicação: 2020 Tipo de documento: Article