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Title:           An open label, randomised controlled trial of rifapentine versus rifampicin based short course regimens for the treatment of latent tuberculosis in England: the HALT LTBI pilot study
Subject:         BMC Infectious Diseases, 2021, doi:10.1186/s12879-021-05766-9
Keywords:        Tuberculosis,Latent tuberculosis treatment,Randomised controlled trial,Rifapentine
Author:          J. Surey
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     Item: 
      Title: Abstract
      Destination: sectionAbs1
      Children: 
       Item: 
        Title: Background
        Destination: sectionASec1
       Item: 
        Title: Methods
        Destination: sectionASec2
       Item: 
        Title: Results
        Destination: sectionASec3
       Item: 
        Title: Conclusion
        Destination: sectionASec4
       Item: 
        Title: Trial registration
        Destination: sectionASec5
     Item: 
      Title: Keypoints
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     Item: 
      Title: Background
      Destination: sectionSec2
     Item: 
      Title: Methods
      Destination: sectionSec3
      Children: 
       Item: 
        Title: Trial design and inclusion criteria
        Destination: sectionSec4
       Item: 
        Title: Outcomes assessments
        Destination: sectionSec5
        Children: 
         Item: 
          Title: Primary outcome: treatment completion
          Destination: sectionSec6
       Item: 
        Title: Secondary outcomes
        Destination: sectionSec7
        Children: 
         Item: 
          Title: Mars
          Destination: sectionSec8
         Item: 
          Title: Adverse events
          Destination: sectionSec9
         Item: 
          Title: Data collection and statistical analysis
          Destination: sectionSec10
     Item: 
      Title: Results
      Destination: sectionSec11
      Children: 
       Item: 
        Title: Primary outcome
        Destination: sectionSec12
       Item: 
        Title: Secondary outcomes
        Destination: sectionSec13
        Children: 
         Item: 
          Title: Adherence using MARS™ tool
          Destination: sectionSec14
         Item: 
          Title: Adverse events
          Destination: sectionSec15
         Item: 
          Title: Blood testing and hepatoxicity
          Destination: sectionSec16
     Item: 
      Title: Discussion
      Destination: sectionSec17
     Item: 
      Title: Conclusion
      Destination: sectionSec18
     Item: 
      Title: Supplementary Information
      Destination: sectionSec19
     Item: 
      Title: Abbreviations
      Destination: sectionabr1
     Item: 
      Title: Acknowledgements
      Destination: section1
     Item: 
      Title: Authors’ contributions
      Destination: section2
     Item: 
      Title: Funding
      Destination: section3
     Item: 
      Title: Availability of data and materials
      Destination: section4
     Item: 
      Title: Ethics approval and consent to participate
      Destination: sectionFPar1
     Item: 
      Title: Consent for publication
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     Item: 
      Title: Competing interests
      Destination: sectionFPar3
     Item: 
      Title: Author details
      Destination: section5
     Item: 
      Title: References
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     Item: 
      Title: Publisher’s Note
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                  <pdfaSchema:schema>PDF/A ID Schema</pdfaSchema:schema>
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                     <rdf:Seq>
                        <rdf:li rdf:parseType="Resource">
                           <pdfaProperty:category>internal</pdfaProperty:category>
                           <pdfaProperty:description>Part of PDF/A standard</pdfaProperty:description>
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                        <rdf:li rdf:parseType="Resource">
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                           <pdfaProperty:description>Amendment of PDF/A standard</pdfaProperty:description>
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                        <rdf:li rdf:parseType="Resource">
                           <pdfaProperty:category>internal</pdfaProperty:category>
                           <pdfaProperty:description>Conformance level of PDF/A standard</pdfaProperty:description>
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