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Endnote 5 x8

Manufactured by Clarivate
Sourced in United States

EndNote (V. X8) is a reference management software that allows users to easily collect, organize, and format citations and bibliographies. It provides a centralized platform for managing research sources and integrating them seamlessly into written documents.

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Lab products found in correlation

5 protocols using endnote 5 x8

1

Systematic Literature Review Protocol

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All of the retrieved citations were imported to EndNote (V. X8; Clarivate Analytics, Philadelphia, PA) after searching in the relevant databases. The title and abstract (if available) of each unique citation were screened by one reviewer (NM) according to the prespecified inclusion and exclusion criteria. The final stage of the screening of the articles (full-text review) was carried out by the two researchers (NM and LD). The researchers (NM and LD) independently extracted relevant data from the articles. In cases of disagreements, the researchers’ views on the elimination of the studies were compared in order to reach a consensus. There were few discrepancies in the data extractors’ views.
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2

Systematic Review of Chagas Latency

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After the search, all identified studies were uploaded and de‐duplicated in EndNote VX8 (Clarivate Analytics, PA, USA). Covidence systematic review software (Veritas Health Innovation, Melbourne, Australia) was used for screening and full‐text review. See eMethods (Supporting Information) for a list of Ovid and PubMed MEDLINE search strategy. Through Covidence, a Preferred Reporting Items for Systematic Reviews and Meta‐Analyses (PRISMA) flow diagram was generated with the number of results found, number excluded during title/abstract screening, and number excluded during full‐text assessments and methodological appraisals, along with reasons for exclusion. Other sources searched included ClinicalTrials.gov (United States National Library of Medicine) and the World Health Organization International Clinical Trials Registry Platform (ICTRP, <http://www.who.int/ictrp/en/>).
Additional details on the systematic review protocol are already published (https://journals.lww.com/jbisrir/Fulltext/2019/10000/Duration_and_determinants_of_Chagas_latency__an.9.aspx). Systematic review registration number: PROSPERO CRD42019118019.
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3

Systematic Review Protocol Screening

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All identified citations were collated and uploaded to EndNote (V.X8; Clarivate Analytics, London, UK) to remove duplicate reports. Titles and abstracts were screened by two independent reviewers (SZ and XZ) to assess whether the inclusion criteria were met. Full-text versions of the selected studies were retrieved and assessed in detail against the inclusion criteria; those that did not meet the inclusion criteria were excluded, and the reasons for exclusion are summarised in the flowchart. Studies selected for inclusion were critically appraised. The search results are presented in a PRISMA flow diagram. Disagreements between the researchers were resolved through discussion or by discussion with a third researcher (KL).
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4

Systematic Review Screening Protocol

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Search results were first collated and uploaded into the citation manager, Endnote V.X8.2 (Clarivate Analytics, Philadelphia, Pennsylvania, USA) and then uploaded to Covidence (Veritas Health Innovation Ltd, Melbourne, Australia), a screening and extraction tool for systematic reviews. Both tools were used to remove duplicates. Two independent reviewers (MC and AG) then screened titles and abstracts for assessment against the inclusion criteria. The full texts of selected citations were retrieved and assessed in detail against the inclusion criteria by two independent reviewers. This data extraction tool was developed by the reviewers (see table 2). Any disagreements between reviewers were resolved through discussion. When full text was not available (eg, conference abstracts), a decision was made to contact authors for further information (eg, if text met majority of predefined inclusion criteria and was missing one key piece of evidence).
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5

Systematic Literature Screening Protocol

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Studies were selected for inclusion using a two-step process: one researcher (MO) screened titles (and abstracts when necessary) to remove duplicates using data management software (EndNote V.X8.2, Clarivate Analytics). Following deduplication, titles and abstracts were screened to determine study eligibility. To ensure the validity of the process, one reviewer (MO) and a second reviewer (NC) each independently screened a random sample of 10% of abstracts; screening results were double-checked by a third reviewer (SL). After resolving disagreements and achieving consensus, the remainder of the screening was undertaken by a single author (MO). Following initial decisions on papers for inclusion, two review authors (MO and SL) each independently reviewed full-text articles against all inclusion and exclusion criteria and resolved disagreements through discussion in order to achieve consensus.
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