Comparison of Huntleigh Dopplex DMX Digital Doppler Arterial Waveform With the Gold Standard of Ultrasound Duplex Arterial Waveform
NCT ID: NCT05373875
Last Updated: 2022-07-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
17 participants
OBSERVATIONAL
2019-01-11
2019-05-03
Brief Summary
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This study aims to compare the audible and visual waveform traces on the Huntleigh Dopplex with the gold standard of ultrasound duplex to assess the accuracy of the trace using diagnostic measurements and the ability of clinicians to correctly identify audible and visual waveforms.
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Detailed Description
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Audible and visual traces from duplex and the Huntleigh will be downloaded. Vascular trainee's in the 1st, 2nd and 3rd years of the scientist training programme and senior vascular scientists will be instructed on predefined waveforms. Audible waveforms and visual traces from the Huntleigh Dopplex will be separated and ordered randomly using a random number generator. Clinicians will listen to waveform recordings, assess visual traces and will be asked to describe them and also determine if this signifies the presence or absence of disease. Results will be analysed using descriptive statistics.
Diagnostic measurements will be taken including pulsatility and resistive index will be calculated to assess for agreement or significant difference between measurements taken on the Huntleigh Dopplex and Duplex ultrasound.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Interventions
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Doppler ultrasound
Doppler to listen and classify the arterial signal in the ankle and arm (Ankle brachial pressure index (ABPI))
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Under the age of 18,
* Known allergy to coupling gel,
* Unable to give consent,
* Pedal pulses are not detectable will be excluded from this study,
* Persons interpreting waveforms will be excluded if they reported having any hearing or visual impairment.
Full Set of Project Data IRAS Version 5.9.1 10
18 Years
ALL
No
Sponsors
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University Hospitals Bristol and Weston NHS Foundation Trust
OTHER
Responsible Party
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Principal Investigators
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Teresa Robinson
Role: PRINCIPAL_INVESTIGATOR
University Hospitals Bristol and Weston NHS Foundation Trust
Locations
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University Hospitals Bristol and Weston NHS Foundation Trust
Bristol, , United Kingdom
Countries
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Other Identifiers
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DT/2018/6670
Identifier Type: -
Identifier Source: org_study_id
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