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Emerging Indications for Hyperbaric Oxygen Treatment: Registry Cohort Study
To gather more data on HBO2 applications, outcome data from multiple centers need to be combined, but until 2011, no major academic registry existed to record treated cases and to track outcomes [5,6].
The International Registry for Hyperbaric Oxygen Treatment was formed to gather consistent outcome data from multiple centers [5]. The registry’s goal is to improve the use of HBO2 through evidence-based medicine.
Interact J Med Res 2024;13:e53821
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In this project, we report on the migration of data collected in the Swiss Mother and Child HIV Cohort Study (Mo CHi V) from Oracle SQL (Oracle Corp) to REDCap. Mo CHi V is a multicenter longitudinal cohort study with approximately 100,000 data records dating back to the early 1980s [19-21]. Data have been prospectively collected via paper forms all over Switzerland submitted by mail to the data center of the Swiss HIV Cohort Study, where data managers transfer the data manually to the Oracle database.
JMIR Form Res 2023;7:e44567
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In light of these challenges, we aimed to explore the applicability and usability of electronic health diary data collected by the Swiss Multiple Sclerosis Registry (SMSR) during a week-long health diary campaign. Specifically, we aimed to compare the characteristics of the participants in the health diary campaign with eligible nonparticipants of the SMSR campaign (aim 1).
JMIR Mhealth Uhealth 2022;10(10):e38709
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The Indigo System in Acute Lower-Limb Malperfusion (INDIAN) Registry: Protocol
The Indigo System in Acute Lower-Limb Malperfusion (INDIAN) Registry was intended as a national platform where every physician could register his or her own data procedure.
A total of 150 patients suffering from acute lower limb malperfusion will be recruited in order to prove safety and efficacy of the Indigo System. All participating centers have extensive experience in this kind of disease.
JMIR Res Protoc 2019;8(3):e9972
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