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The aim of the study is to assess the effect of Rotating Magnetic Therapy on Diabetic Peripheral Neuropathy using Nerve conduction velocity examination.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control group | Sham Comparator | Mecobalamine 0.5mg, tid |
|
| Rotating Magnetic Therapy | Experimental | Rotating Magnetic Therapy 30min,bid + Mecobalamine 0.5mg, tid |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Rotating Magnetic Therapy | Device | Rotating Magnetic Therapy 30min, bid |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Nerve conduction velocity examination | the change of Nerve conduction velocity examination | 1 month |
| Measure | Description | Time Frame |
|---|---|---|
| MNSI | Michigan Neuropathy Screening Instrument | 1 month |
| Glycosylated serum albumin | the change of Glycosylated serum albumin | 1 month |
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Inclusion Criteria:
- 1. Volunteer to participate and sign informed consent prior to the study 2. Patients with type 2 diabetes, who met WHO1999 diagnostic criteria, had diabetes distal symmetrical multiple neuropathy (1) clear history of diabetes; (2) neuropathy at or after diagnosis of diabetes;(3) clinical manifestations and signs are consistent with DPN;(4) have clinical symptoms (pain, numbness, paresthesia, etc.), 5 examination (ankle reflex, acupuncture pain sense, vibration sense, pressure sense, temperature sense) any 1 abnormal;If there were no clinical symptoms, 2 of the 5 examinations were abnormal.(5) exclude other causes of neuropathy).
3. HbA1c<7.5%, the hypoglycemic regimen was stable for 3 months 4. No acute complications, such as diabetic ketoacidosis, diabetic hyperosmolar syndrome, etc.
Exclusion Criteria:
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| ID | Term |
|---|---|
| C019476 | mecobalamin |
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| Mecobalamin |
| Drug |
mecobalamine 0.5mg,tid |
|