2009
DOI: 10.3310/hta13280
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A randomised controlled trial to compare minimally invasive glucose monitoring devices with conventional monitoring in the management of insulin-treated diabetes mellitus (MITRE)

Abstract: How to obtain copies of this and other HTA programme reports An electronic version of this publication, in Adobe Acrobat format, is available for downloading free of charge for personal use from the HTA website (www.hta.ac.uk). A fully searchable CD-ROM is also available (see below).Printed copies of HTA monographs cost £20 each (post and packing free in the UK) to both public and private sector purchasers from our Despatch Agents.Non-UK purchasers will have to pay a small fee for post and packing. For Europea… Show more

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Cited by 22 publications
(15 citation statements)
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References 209 publications
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“…These were comfort during the health intervention [11,12], the intervention being quick to undertake [13], the intervention being easy to undertake [13,14], and the intervention being perceived as effective [12]. From these four identified factors, five questionnaire items designed to measure perceived acceptability were developed, as follows: two items measured how comfortable participants felt using the dry decontamination product (e.g.…”
Section: Methodsmentioning
confidence: 99%
“…These were comfort during the health intervention [11,12], the intervention being quick to undertake [13], the intervention being easy to undertake [13,14], and the intervention being perceived as effective [12]. From these four identified factors, five questionnaire items designed to measure perceived acceptability were developed, as follows: two items measured how comfortable participants felt using the dry decontamination product (e.g.…”
Section: Methodsmentioning
confidence: 99%
“…Patterns of blood glucose were observed over 2-7 days before advising insulin dose changes depending on frequency of testing and blood glucose level. Treatment algorithms are available in the study protocol [21]. Attention control subjects attended research visits at 4, 8 and 12 weeks, where SMBG results were downloaded and used as the basis for feedback.…”
Section: Trial Designmentioning
confidence: 99%
“…Although this system originally gained FDA approval (2001), it was removed from the market in 2008 due to technical issues regarding accuracy. Side effects such as skin irritation, and reported issues with ease-of-use require resolution for the successful adoption of this type of system over existing technologies (Newman, 2009).…”
Section: Biological and Chemical Sensingmentioning
confidence: 99%