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The Early Intervention and Prevention of Diabetes Foot

The Early Intervention and Prevention of Diabetes Foot

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03133819
Enrollment
400
Registered
2017-04-28
Start date
2016-11-30
Completion date
2019-04-30
Last updated
2017-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes; Neuropathy, Polyneuropathy (Manifestation)

Brief summary

Peripheral neuropathy is just assessed by determination of Vibration sensation, pressure sensation, superficial pain or temperature. The most commonly used technique for diagnosis of peripheral neuropathy is nervous conduction (NC) and electromyography (EMG). But EMG/NC is bothersome and techniques using electric currents to measure NC and needles to study muscle innervations are uncomfortable. Quantitative NeuroSensory Testing (QST) is essential in the evaluation of small-caliber A-delta and C-fibers, the primary transmitters of thermal and pain sensation. QST can demonstrate neurosensory abnormalities when it is non-invasive test, selective to small fibers despite negative EMG/NCV finding. The investigators predict QST can be used for the early diagnosis and follow-up of small-fiber neuropathy in diabetes patients. The investigators also predict the early evaluation of diabetes neuropathy with QST can reduce the diabetes patient progress to advance stage of DM foot or limb amputation.

Detailed description

Patients will be divide into 4 groups (groups 1 to 4 will be divided by Q-Sense QST (TSA II) . The patient groups will be defined as the followings: 1. Group 1: 100 diabetes patients without neuropathy, Q-Sense normal. 2. Group 2: 100 diabetes patients with neuropathy, Q-Sense abnormal but no evidence of PAOD. 3. Group 3: 100 diabetes patients with neuropathy, Q-Sense abnormal , PAOD (+), but no foot ulceration 4. Group 4: 100 diabetes patients with neuropathy, PAOD(+) , and foot ulceration QST will perform using the Medoc device (TSA2001/VSA3001) following previous published procedures.

Interventions

DEVICEQ-Sense_QST (TSA II)

QST will perform using the Medoc device (TSA2001/VSA3001) following previous published procedures. The measurement will perform on the thenar eminence of the dominant hand and the lateral distal aspect of the foot dorsum of the same side.

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Group 1: 100 diabetes patients without neuropathy, Q-Sense normal. * Group 2: 100 diabetes patients with neuropathy, Q-Sense abnormal but no evidence of PAOD. * Group 3: 100 diabetes patients with neuropathy, Q-Sense abnormal , PAOD (+), without foot ulceration. * Group 4: 100 diabetes patients with neuropathy, PAOD (+), and foot ulceration.

Exclusion criteria

* Poorly controlled hypertension (SBP≥150 under regular medical treatment) * Thyroid disease * Pregnancy * Have been diagnosed malignancy * Liver cirrhosis

Design outcomes

Primary

MeasureTime frameDescription
Glycohemoglobin (HbA1c)month 0, 6, 12To see the correlation between diabetes neuropathy (by Q sense measurement) and glycemic control status ( at baseline, 6 months and 12 months).
Lipid profilemonth 0,6,12To see the correlation between diabetes neuropathy (by Q sense measurement) and lipid profile ( at baseline, 6 months and 12 months).
Diabetes nephropathy ( macro-albuminuria (UACR ≧300 mg/g) ,micro-albuminuria (UACR: 30 - 300 mg/g))month 0,6,12To see the correlation between diabetes neuropathy (by Q sense measurement) and albuminuria status ( at baseline, 6 months and 12 months). Check the albuminuria status by the criteria (macro-albuminuria (UACR ≧300 mg/g) ,micro-albuminuria (UACR: 30 - 300 mg/g))
Peripheral arterial occlusive diseasemonth 0,6,12To see the correlation between diabetes neuropathy (by Q sense measurement) and severity of peripheral arterial occlusive disease ( at baseline, 6 months and 12 months).

Secondary

MeasureTime frameDescription
major lower leg events ( lower leg amputation or revascularization)month 0,6,12To see the correlation between diabetes neuropathy (by Q sense measurement) and major lower leg events including lower leg amputation or revascularization) ( at baseline, 6 months and 12 months).
Major cardiac events ( myocardial infarction, strokes and cardiac related death)month 0,6,12To see the correlation between diabetes neuropathy (by Q sense measurement) and major cardiac events including myocardial infarction, strokes and cardiac related death)( at baseline, 6 months and 12 months.
Diabetes footmonth 0, 6, 12To see the correlation between diabetes neuropathy (by Q sense measurement) and diabetes foot, foot ulceration ( at baseline, 6 months and 12 months).

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026