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During the implementation of this BIAN, for the first time, Indonesia used an electronic immunization registry (EIR) capturing individual-level records [5] and replacing paper-based records as the latter were shown previously to include inaccuracies due to inexact, incomplete data and late reporting [10-12].
EIRs as part of an immunization information system are a tool designed to provide information on immunization programs’ target populations.
Interact J Med Res 2025;14:e53849
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This is a prospective, observational, multicenter, hospital-intensive monitoring, and continuous registry study. We used the SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) checklist when writing our report [23]. The study flowchart is shown in Figure 1.
Study flowchart. ADR: adverse drug reaction; CRF:case report form; PDL: Pudilan xiaoyan oral liquid.
JMIR Res Protoc 2025;14:e65789
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We conducted a cross-sectional analysis using Clinical Trials.gov, a trial registry and results database maintained by the US National Library of Medicine. We sourced data from the Clinical Trials Transformation Initiative Aggregate Analysis of Clinical Trials.gov (CTTI AACT) [15], which allows open access to the complete set of trials registered in Clinical Trials.gov, including additional fields that are not readily available in direct exports from Clinical Trials.gov.
J Med Internet Res 2024;26:e57750
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The Zindagi Mehfooz (safe life; ZM) electronic immunization registry (EIR) is a comprehensive suite of digital health interventions that aims to improve equitable access, timeliness, and coverage of child immunizations through a smartphone-based app for vaccinators, web-based dashboards for supervisors and managers, text message alerts and reminders for caregivers, and a call center. It has been implemented at scale in Sindh Province, Pakistan.
J Med Internet Res 2024;26:e52792
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A review of the Australian New Zealand Clinical Trials Registry indicated that of 13,666 trials registered from 2005 to 2017 in the registry, 6168 (45%) included a PROM [9].
PROMs in clinical trials are important for decision-making among the stakeholders involved, especially in medical device-related trials to measure adverse events and other negative outcomes to assess the safety of a medical device [10].
JMIR Res Protoc 2024;13:e52572
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Integration of a patient-centered digital registry and CDSS for psychosis could be equally transformative and give parity of esteem to one of the most common and disabling sets of mental health disorders—psychosis—where there is already a well-developed national infrastructure of EIP services.
To achieve this paradigmatic change in mental health care, our aim is to develop, evaluate, and establish a national psychosis registry and CDSS, known as EPICare (Early Psychosis Informatics into Care) in 3 stages.
JMIR Res Protoc 2024;13:e50177
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Thailand has maintained a national citizen registry linked to national health databases since 1993 [20]. Specialized registries have been established for COVID-19 testing, COVID-19 cases, and COVID-19 vaccination [21]. By linking these records, we examined a dynamic cohort of the Thai population to assess the durability of VE of heterologous vaccine sequences, providing insights for future pandemics.
JMIR Public Health Surveill 2024;10:e48255
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Here we use a community-based registry in the United States to describe participant-reported data on COVID-19 vaccine side effects and breakthrough infections in people with diabetes and examine whether diabetes medicine use affects the risk of developing vaccine side effects.
JMIR Diabetes 2024;9:e45536
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The purpose of this communication is to describe a roadmap for developing the Venous Access: National Guideline and Registry Development (VANGUARD) Coordinated Registry Network (CRN) to meet these challenges and thus improve the quality of care provided to patients requiring CVADs.
J Med Internet Res 2023;25:e43658
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