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  1. 341
    “…Clinical trials of contraceptives have often differed in their study designs, making cross-trial comparisons difficult. …”
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    Variability in Contraceptive Clinical Trial Design and the Challenges in Making Comparisons Across Trials
  2. 342
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    Gender effect in the ITALUNG screening trial. A comparison with UKLS and other trials
  3. 343
    “…In this study using electrocorticographic (ECoG) signals, we manipulated the predictability of oddball sound sequences with two objectives: (i) Uncovering the computational process underlying trial-by-trial variations of the cortical responses. …”
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    Dynamics of Oddball Sound Processing: Trial-by-Trial Modeling of ECoG Signals
  4. 344
    “…Corresponding scientific publications were searched via clinical trial registries, PubMed (MEDLINE), and Google. RESULTS: Overall, 330 clinical trials were authorized in 2012 of which 232 trials were completed for more than 1 year in June 2020. …”
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    Publication of clinical trials on medicinal products: follow-up on trials authorized in Hungary
  5. 345
    “…Over the past decade, methodologic tools have been developed to inform the design, analysis, reporting, and interpretation of patient-reported outcome data from clinical trials. We formed the PROTEUS-Trials Consortium (Patient-Reported Outcomes Tools: Engaging Users and Stakeholders) to disseminate and implement these methodologic tools. …”
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    The PROTEUS-Trials Consortium: Optimizing the use of patient-reported outcomes in clinical trials
  6. 346
    por Peto, Leon, Horby, Peter, Landray, Martin
    Publicado 2022
    “…The Randomised Evaluation of COVID-19 Therapy (RECOVERY) Trial was set up in March 2020 to evaluate treatments for people hospitalised with COVID-19. …”
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    Establishing COVID-19 trials at scale and pace: Experience from the RECOVERY trial
  7. 347
    “…CONCLUSION: Patients can be recruited to a trial of this design. These data will inform the design of further trials in post-stroke fatigue.…”
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    Post stroke intervention trial in fatigue (POSITIF): Randomised multicentre feasibility trial
  8. 348
    “…METHODS: TARDIS was an international prospective randomised open-label blinded-endpoint trial assessing one month of intensive versus guideline antiplatelet therapy in patients with acute non-cardioembolic stroke or TIA. …”
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    Optimising the analysis of vascular prevention trials: Re-Assessment of the TARDIS trial, the first prevention trial to adopt an ordinal primary outcome measure()
  9. 349
    “…BACKGROUND/OBJECTIVE: Despite the intuitive attractiveness of bringing research to participants rather than making them come to central study sites, widespread decentralized enrollment has not been common in clinical trials. METHODS: The need for clinical research in the context of the COVID-19 pandemic, along with innovations in technology, led us to use a decentralized trial approach in our Phase 2 COVID-19 trial. …”
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    From a decentralized clinical trial to a decentralized and clinical-trial-in-a-box platform: Towards patient-centric and equitable trials
  10. 350
    “…PURPOSE: The co.21 Colon Health and Life-Long Exercise Change (challenge) trial undertaken by the National Cancer Institute of Canada Clinical Trials Group (ncic ctg) is designed to determine the effects of a structured pa intervention on outcomes for survivors of high-risk stage ii or iii colon cancer who have completed adjuvant therapy within the previous 2–6 months. …”
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    The Colon Health and Life-Long Exercise Change trial: a randomized trial of the National Cancer Institute of Canada Clinical Trials Group
  11. 351
    “…OBJECTIVES: To present an adapted Clinical Trial Processor (CTP) test set-up for receiving, anonymising and saving Digital Imaging and Communications in Medicine (DICOM) data using external input from the original database of an existing clinical study information system to guide the anonymisation process. …”
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    Implementation of an anonymisation tool for clinical trials using a clinical trial processor integrated with an existing trial patient data information system
  12. 352
    por Whitham, Diane, Duley, Lelia
    Publicado 2013
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    Evaluation of a site selection questionnaire for the recruitment of trial sites into multi-centre trials: experiences from the nottingham clinical trials unit
  13. 353
    “…To identify additional eligible randomised controlled trials (RCTs) for a Cochrane systematic review of strategies to improve retention in RCTs, we conducted a survey of UK clinical trials units (CTUs) and made contact with RCT methodologists. …”
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    Identifying additional studies for a systematic review of retention strategies in randomised controlled trials: making contact with trials units and trial methodologists
  14. 354
    “…RESULTS: Thirty-one current Consolidated Standards of Reporting Trials group affiliates were invited for survey participation (February 2015). …”
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    Sharing some interim data in trial monitoring can mislead or unmask trial investigators: A scenario-based survey of trial experts
  15. 355
    “…INTRODUCTION: Dissemination of results of randomised controlled trials is traditionally limited to academic and professional groups rather than clinical trial participants. …”
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    Study within a trial (SWAT) protocol. Participants' perspectives and preferences on clinical trial result dissemination: The TRUST Thyroid Trial experience
  16. 356
    “…BACKGROUND: Randomised controlled trials are the cornerstone of evidence-based health care, yet many trials struggle with recruitment and retention. …”
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    Doing trials within trials: a qualitative study of stakeholder views on barriers and facilitators to the routine adoption of methodology research in clinical trials
  17. 357
    “…Objective: Clinical trials have emerged as the main force in driving the development of medicine. …”
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    Clinical Trials Focusing on Drug Control and Prevention of Ventilator-Associated Pneumonia: A Comprehensive Analysis of Trials Registered on ClinicalTrials.gov
  18. 358
    Publicado 2019
    Materias: “…Clinical Trials…”
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    Treatment of Symptomatic Convergence Insufficiency in Children Enrolled in the Convergence Insufficiency Treatment Trial–Attention & Reading Trial: A Randomized Clinical Trial
  19. 359
    “…BACKGROUND: Retention (participants completing a trial) is a persistent, and often under-studied, challenge within clinical trials. …”
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    What influences communication about retention in randomised trials: a multi-trial, theory-based analysis exploring trial staff perspectives
  20. 360
    “…This study protocol describes the design and conduct of this trial. The YOGA study is a phase III, single-centre, parallel, superiority, randomised, active-controlled trial which will be conducted in Hobart, Australia. …”
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    A Randomised Controlled Trial of YOGa and Strengthening Exercise for Knee OsteoArthritis: Protocol for a Comparative Effectiveness Trial (YOGA Trial)
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