2018
DOI: 10.1016/j.jvsv.2018.03.005
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Individualised Versus Standard Duration of Elastic Compression Therapy for Prevention of Post-Thrombotic Syndrome (IDEAL DVT): A Multicentre, Randomised, Single-Blind, Allocation-Concealed, Non-Inferiority Trial

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Cited by 12 publications
(21 citation statements)
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“…Time to compression was within 24 hours of the diagnosis. There were three prespecified protocols for compression in the acute phase . Initial compression was associated with a 15% relative reduction of (predominantly irreversible) skin signs.…”
Section: Thrombus Resolutionmentioning
confidence: 99%
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“…Time to compression was within 24 hours of the diagnosis. There were three prespecified protocols for compression in the acute phase . Initial compression was associated with a 15% relative reduction of (predominantly irreversible) skin signs.…”
Section: Thrombus Resolutionmentioning
confidence: 99%
“…The incidences of PTS were 28.9% and 27.8%, respectively. The absolute difference was 1.1% (95% CI upper limit of 7.2%), thereby not exceeding the upper limit of the predefined noninferiority margin of 7.5% . The IDEAL study essentially confirmed the findings of the previous management study, concluding that individualized shortened duration of compression for 6 months is similar to standard duration of compression for 24 months.…”
Section: Barriers To Progress and Future Perspectivesmentioning
confidence: 99%
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“…This study was an a priori-planned substudy of the IDEAL DVT study, which has been described in detail previously [15]. In short, the IDEAL DVT study was a multicenter randomized controlled trial that started in April 2011 and was concluded in July 2017.…”
Section: Study Design and Population Centermentioning
confidence: 99%