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UnknownNCT03378024

Evaluate the Correlation of NIRS, ABI, Exercise, baPWV and Albuminuria With Peripheral Artery Occlusion Disease (PAD) and Other Atherosclerosis Outcomes

To Evaluate the Correlation of Near Infrared Spectroscopy, ABI, Exercise Test, baPWV and Microalbuminuria With Peripheral Artery Occlusion Disease and Other Atherosclerosis Outcome

Status
Unknown
Phase
Study type
Observational
Enrollment
650 (estimated)
Sponsor
Chang Gung Memorial Hospital · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Accepted

Summary

By utilizing Near infrared spectroscopy (NIRS), the local blood flow, tissue oxygenation (StO2), and recovery time of ischemic leg; can be determined. It is reasonable to standardize an easy, simple and safe Active Pedal Plantarflexion (APP) exercise test working load which can achieve the lowest StO2 and other parameters in ischemic leg through observation of NIRS. After standardized of an effective APP test, a determination of a new cutoff value of resting ABI in diagnosing PAD can probably be searched. Analysing the correlation of baPWV with ABI, atherosclerosis risk factors and parameters with atherosclerosis outcome. Observation the Sequential changes of baPWV, ABI and microalbuminuria after managing the atherosclerosis risks, and analyze their influence on the outcome of PAD, coronary artery disease(CAD) and cerebral vascular disease(CVA) outcomes.

Detailed description

Exercise testing by Active Pedal Plantar flexion: The investigators plan to collect 140 cases: 1. Healthy subjects with no apparent atherosclerotic risk \[\< 65 y/o, no diabetic mellitus (DM), no hypertension, or no hyperlipidemia, not obese, not current smoker, no smoking history \>10 years\] 4(n=5) 2. Patients at risks (e.g. hypertension, hyperlipidemia) (n=5) but without DM, 3. Type 1 and Type 2 DM patients with normal ABI( \>1.0)and normal Toe-brachial index (TBI) (\> 0.6) without intermittent claudication(by Edinburgh claudication questionnaire), nor PAD diagnosis (n= 10) 4. DM normal ABI\>1.0 and normal TBI (\> 0.6) with suspected symptoms (intermittent claudication, non healing ulcer) (n=10), 5. DM normal or borderline ABI( \>1, 0.91\~0.99) but low TBI (\< 0.6), or with suspected symptoms (intermittent claudication, non healing ulcer) (n=20), 6. DM patients with borderline ABI (0.91-0.99) (n=50) with or without leg symptoms, 7. DM patients abnormal Low ABI (\<0.9) (n=30) with or without leg symptoms, 8. DM patients abnormal high ABI (\> 1.3) (n=10)with or without leg symptoms, Post-exercise ABI with APP, and NIRS examination during APP exercise test will be performed. The investigators also plan to collect 500 cases of nonpregnant, ≥ 40 years old DM patients, obtained baPWV and the resting ABI by oscillometric device (Omron colin, Japan). The investigators will apply this novel technique to assess the extent of arteriosclerosis and atherosclerosis by oscillometric device in our DM patient without PAD (ABI \>0.9). Collect baseline characteristics and follow up annual data: Age, sex, body weight, height, BMI, waist circumferences, history of smoking (ex-smoker, current), coexisting hypertension, hyperlipidemia, DM duration, presence of chronic DM complications of neuropathy, retinopathy (by fundus camera), nephropathy (cr, estimate glomerular filtration rate(eGFR), proteinuria, microalbuminuria). The biochemistry data involving atherosclerotic risk including: systolic blood pressure, diastolic pressure, mean pulse pressure, HbA1c, total cholesterol, LDL-Cholesterol(LDL-C), HDL-Cholesterol(HDL-C), triglyceride, creatinine, microalbuminuria,, high sensitive C-Reactive Protein (hs CRP), baseline EKG all will be collected. All the above data will be followed up annually for 3 years to analyze the correlation of progressive change of baPWV, ABI and microalbuminuria with the atherosclerosis event and mortality.

Conditions

Interventions

TypeNameDescription
DEVICEoscillometric (Omron Colin co)fast measurements of the brachial-ankle pulse wave velocity (baPWV) and the resting ankle-brachial index(ABI) with the oscillometric method (Omron Colin co, Japan)

Timeline

Start date
2016-12-01
Primary completion
2019-04-30
Completion
2019-04-30
First posted
2017-12-19
Last updated
2017-12-19

Source: ClinicalTrials.gov record NCT03378024. Inclusion in this directory is not an endorsement.