PAD Clinical Trial
— PWViOfficial title:
Pulse Wave Velocity Imaging in the Assessment of PAD
NCT number | NCT03516383 |
Other study ID # | 16-028 |
Secondary ID | |
Status | Withdrawn |
Phase | |
First received | |
Last updated | |
Start date | June 2016 |
Est. completion date | June 2017 |
Verified date | April 2018 |
Source | St. Michael's Hospital, Toronto |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to predict the outcome of peripheral revascularization surgery by use of a new technology developed by our team, Pulse Wave Velocity imaging (PWVI), which has the capability to detect pulse transit time (PTT), and pulse wave velocity (PWV). This PWVI will be compared against known gold standards pre and post lower extremity limb revascularization and used to evaluate outcomes. Specifically, is leg PWV different among those with or without PAD, and is leg PWV different among those who undergo revascularization surgery and those who do not? This study represents the first clinical pilot study of the device with the aim to expand study participant numbers in future research and to eventually develop a PAD screening tool. This would be the first of its kind ever described.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | June 2017 |
Est. primary completion date | June 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 64 Years |
Eligibility |
Inclusion Criteria Group 1. Control (n=10) - ABI of 0.9 < ABI < 1.2 - 50 - 90 years of age - Participants who understand the study and are able to give consent - Participants who can be followed by the same investigating team for the whole period of their participation in the study Group 2. Experimental (n=10) - ABI < 0.6, confirmed PAD - 50 - 90 years of age - In-patients or out-patients - Participants who understand the study and are able to give consent - Participants who can be followed by the same investigating team for the whole period of their participation in the study Exclusion Criteria Group 1. Control (n=10) - Diabetics - Smokers - Body mass index (BMI) > 35 Group 2. Experimental (n=10) - Diabetics - Smokers - Advanced lymphedema or dermatoliposclerosis - BMI > 35 |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
St. Michael's Hospital, Toronto | Ryerson University |
Aboyans V, Criqui MH, Abraham P, Allison MA, Creager MA, Diehm C, Fowkes FG, Hiatt WR, Jönsson B, Lacroix P, Marin B, McDermott MM, Norgren L, Pande RL, Preux PM, Stoffers HE, Treat-Jacobson D; American Heart Association Council on Peripheral Vascular Disease; Council on Epidemiology and Prevention; Council on Clinical Cardiology; Council on Cardiovascular Nursing; Council on Cardiovascular Radiology and Intervention, and Council on Cardiovascular Surgery and Anesthesia. Measurement and interpretation of the ankle-brachial index: a scientific statement from the American Heart Association. Circulation. 2012 Dec 11;126(24):2890-909. doi: 10.1161/CIR.0b013e318276fbcb. Epub 2012 Nov 16. Review. Erratum in: Circulation. 2013 Jan 1;127(1):e264. — View Citation
Beckman JA, Jaff MR, Creager MA. The United States preventive services task force recommendation statement on screening for peripheral arterial disease: more harm than benefit? Circulation. 2006 Aug 22;114(8):861-6. — View Citation
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---|---|---|---|---|
Primary | Waveform Imaging using Pulse Wave Velocity | Using new technology to measure tissue viability in surgical participants. | 8 weeks |
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