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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03378024
Other study ID # CMRPG2F0181
Secondary ID
Status Enrolling by invitation
Phase N/A
First received May 4, 2017
Last updated December 17, 2017
Start date December 1, 2016
Est. completion date April 30, 2019

Study information

Verified date May 2017
Source Chang Gung Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 650
Est. completion date April 30, 2019
Est. primary completion date April 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- type 1 diabetic patients

- type 2 diabetic patients

Exclusion Criteria:

- Pregnancy

- Critical limb ischemia (gangrene change)

- A permanent pacemaker implant

- Systolic BP = 200 mmHg or diastolic BP =100 mmHg

- Symptomatic orthostatic blood pressure drop = 20 mmHg

- Severe critical aortic stenosis

- Acute medical illness, fever, systemic infection

- Uncontrolled atrial or ventricular dysrhythmias

- Uncontrolled sinus tachycardia= 120/min

- Peripheral venous insufficiency, thrombosis or thrombophlebitis

- Those who has factors known to influence the PWV

- The brachial-ankle PWV could not be measured on the right and left sides

- Orthopedic condition (ankle or foot) that cannot perform an active pedal plantar flexion (APP) technique (arthritis, hemiparesis, balance impairment etc.)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
oscillometric (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)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Chang Gung Memorial Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Define the correlation between NIRS and ABI Analyse the correlation of NIRS with different ABI 12 month
Primary Defined APP exercise ABI criteria for PAD diagnosis Design APP exercise with effective working load to defined ABI criteria for PAD diagnosis 12 month
Primary The correlation of changes of baPWV and the outcome of PAD Analyse the sequential changes of baPWV and the outcome of PAD 12,24 and 36 months
Primary The correlation of changes of exercise ABI and the outcome of PAD Analyse the sequential changes of exercise ABI and the outcome of PAD 12,24 and 36 months
Primary The correlation of changes of albuminuria and the outcome of PAD Analyse the sequential changes of albuminuria and the outcome of PAD 12,24 and 36 months
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