Multicentre Study to Investigate the Performance of the Padd Device in the Assessment of Peripheral Arterial Disease
NCT ID: NCT01633710
Last Updated: 2012-07-04
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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TERMINATED
86 participants
OBSERVATIONAL
2009-05-31
2010-07-31
Brief Summary
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Detailed Description
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In addition to standard questionnaires, participants will undergo bilateral Padd and resting ABPI. CDU will be performed by an accredited vascular technologist who will employ a scoring method consistent between both sites. The vascular technologist will be blind to the Padd and ABPI results. The results obtained with Padd and ABPI will be compared with CDU as the gold standard for this study.
The primary objectives are:
1. Performance: to compare Padd and ABPI for detecting PAD against a gold standard, CDU, performed by an experienced vascular technologist.
2. Safety: to compare adverse events using Padd, ABPI and expert CDU
The secondary objectives are:
1. to compare time taken to perform Padd and ABPI
2. to calculate specificities for Padd and ABPI
3. to investigate the impact of subject posture on the Padd results
4. to determine if skin colour has any impact on Padd performance
There are no treatments or interventions determined exclusively from the Padd readings.
Conditions
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Keywords
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
2. Leicester
* age 70 years or older
* age 50-69 years with a history of smoking, diabetes or peripheral arterial disease
* 50-69 years with at least two peripheral arterial disease risk factors (hyperlipidaemia, hypertension, family history of cardiovascular disease, previous ischaemic event: myocardial infarction, stroke and TIA)
Exclusion Criteria
2. acute deep venous thrombosis, within the previous six months (application of ABPI pressure cuff on legs is not advisable for these patients)
3. skin damage or infection that precludes placement of sensors
4. active psychotic illness or severe cognitive impairment
5. inability to lie supine
50 Years
ALL
No
Sponsors
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University Hospitals, Leicester
OTHER
Responsible Party
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University of Leicester
Principal Investigators
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Kamlesh Khunti, MB BS
Role: PRINCIPAL_INVESTIGATOR
University of Leicester
Locations
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University of Leicester
Leicester, Leicestershire, United Kingdom
Royal Free Hospital
London, London, United Kingdom
Countries
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Other Identifiers
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DDL-2009-01
Identifier Type: -
Identifier Source: org_study_id