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secure web-based randomisation system  (Data Architects Ltd)

 
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    Structured Review

    Data Architects Ltd secure web-based randomisation system
    Schedule of assessments for NULevel trial
    Secure Web Based Randomisation System, supplied by Data Architects Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/secure+web-based+randomisation+system/secure+web+based+randomisation+system/pmc04580361-255-3-16
    Average 90 stars, based on 1 article reviews
    secure web-based randomisation system - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "The NULevel trial of a scalable, technology-assisted weight loss maintenance intervention for obese adults after clinically significant weight loss: study protocol for a randomised controlled trial"

    Article Title: The NULevel trial of a scalable, technology-assisted weight loss maintenance intervention for obese adults after clinically significant weight loss: study protocol for a randomised controlled trial

    Journal: Trials

    doi: 10.1186/s13063-015-0931-7

    Schedule of assessments for NULevel trial
    Figure Legend Snippet: Schedule of assessments for NULevel trial

    Techniques Used: Activity Assay

    Related Articles

    Activity Assay:

    Article Title: The NULevel trial of a scalable, technology-assisted weight loss maintenance intervention for obese adults after clinically significant weight loss: study protocol for a randomised controlled trial
    Article Snippet: A secure web-based randomisation system based on variable-length blocks, provided by Newcastle Clinical Trials Unit via Data Architects Ltd. (Newcastle upon Tyne, UK), is used to ensure concealment of allocation.

    Article Title: Behavioural intervention for weight loss maintenance versus standard weight advice in adults with obesity: A randomised controlled trial in the UK (NULevel Trial)
    Article Snippet: A secure web-based randomisation system based on variablelength blocks, provided by Newcastle Clinical Trials Unit via Data Architects Ltd. (Newcastle upon Tyne, UK), is used to ensure concealment of allocation.



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    Image Search Results


    Primary maternal and perinatal outcome

    Journal: Lancet (London, England)

    Article Title: Planned delivery or expectant management for late preterm pre-eclampsia in low-income and middle-income countries (CRADLE-4): a multicentre, open-label, randomised controlled trial

    doi: 10.1016/S0140-6736(23)00688-8

    Figure Lengend Snippet: Primary maternal and perinatal outcome

    Article Snippet: Participants were recruited from nine hospitals and referral facilities in India and Zambia and randomly assigned to planned delivery or expectant management in a 1:1 ratio by a secure web-based randomisation facility hosted by MedSciNet.

    Techniques: Biomarker Discovery

    Secondary maternal outcomes

    Journal: Lancet (London, England)

    Article Title: Planned delivery or expectant management for late preterm pre-eclampsia in low-income and middle-income countries (CRADLE-4): a multicentre, open-label, randomised controlled trial

    doi: 10.1016/S0140-6736(23)00688-8

    Figure Lengend Snippet: Secondary maternal outcomes

    Article Snippet: Participants were recruited from nine hospitals and referral facilities in India and Zambia and randomly assigned to planned delivery or expectant management in a 1:1 ratio by a secure web-based randomisation facility hosted by MedSciNet.

    Techniques:

    Maternal demographic and pregnancy characteristics

    Journal: Bjog

    Article Title: Two‐year follow‐up of infant and maternal outcomes after planned early delivery or expectant management for late preterm pre‐eclampsia ( PHOENIX ): A randomised controlled trial

    doi: 10.1111/1471-0528.17167

    Figure Lengend Snippet: Maternal demographic and pregnancy characteristics

    Article Snippet: The only exclusion criterion to participation was the clinician’s decision to initiate delivery within the subsequent 48 h. After providing written informed consent, women were randomly assigned to planned delivery or expectant management via a secure web‐based randomisation program provided by MedSciNet.

    Techniques: