Efficacy of γ-linolenic Acid and Thioctic Acid in Patients With Diabetic Neuropathy

• Status: Completed
• Trial end date: 2018-07-25
• Target enrollment: 0
• Participant gender: All

Summary

This study was a 12-week, multi-center, randomized, double-blind, double dummy, parallel clinical trial to compare the efficacy of γ-linolenic acid and Thioctic acid in patients with diabetic neuropathy.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Chonbuk National University Hospital
• Treatments: Evening primrose oil; Thioctic Acid

Criteria

Inclusion Criteria:

• Patients who were between 20 years and 75 years at screening

• Patients who were diagnosed with type 2 diabetes and whose HbA1c levels were less than 11% at screening

• Patients with a score of 4 or more on the Visual Analogue Score(VAS)

• One or more of the following items

• If the physical examination score of the Michigan Neuropathy Screening Instrument Score (MNSI) is more than 2 points at the initial screening

• type 2 diabetic patient who complained one or more of pain, burning sensation, numbness, and sensory loss and measured the current perception threshold (CPT) of the peroneal nerve at three frequencies (2000Hz, 250Hz, 5Hz) Anyone whose diabetes mellitus has been diagnosed as diabetic neuropathy

• Patients who decided to voluntarily participate in clinical trials and agreed in writing

Exclusion Criteria:

• Peripheral neuropathy caused by other causes other than diabetes

• Those are suffering from other painful conditions that are so severe that diabetic neuropathy can not be assessed

• If you have a progressive or degenerative neurological disorder

• Patients with a systolic blood pressure(SBP)≥ 160 mmHg or ≤ 100 mmHg or a diastolic blood pressure(DBP) ≥ 95 mmHg or ≤ 60 mmHg

• Patients who were positive for human immunodeficiency virus (HIV), hepatitis B (HBV), or hepatitis C (HCV) test

• patients with liver dysfunction (ALT / AST> 3 times the upper limit of normal)

• Patients with renal dysfunction (Serum creatine> 2.0 mg / dl)

• Patients with thyroid dysfunction (Thyroid and anti-thyroid medications may be included in this study if they are maintained in normal state.)

• Patients with amputation (including toes) or infections of the lower extremities

• The following diseases are clinically significant patients

• Unstable coronary artery disease or peripheral vascular disease

• Liver, kidney, lung, hematologic disease

• Cancer (within 5 years if possible)

• Patients who have suicide attempts or suicidal tendencies and who have a psychiatric history within 6 months before starting the trial

• Patients with substance abuse or chronic alcohol abuse within 2 years prior to taking the test

• Patients who received intravenous steroid injection or topical anesthetic injection within 2 months before participating in the study

• Patients who participated in other studies within 4 weeks before participating in the trial, or who are currently taking medication for other research

• Screening After randomization for 2 weeks (pause period) before screening, antipsychotics, antipsychotics, sleep depressants, antidepressants, antiepileptics, muscle relaxants, analgesics (narcotic analgesics, NSAIDs, tramadol etc.) Patients who received capsaicin or who received percutaneous electrical nerve stimulation therapy (TENS) or acupuncture

• Patients with a history of hypersensitivity or clinically significant hypersensitivity reactions to this drug substance and soybean oil, soy or peanut

• Patients with clinically significant skin disease or severe skin irritability

• Pregnant or lactating women

• patients suffering from schizophrenia or those who are treated with chloropromazine, mesoridazine, thioridazine, fluphenazine, perphenazine, trifluoperazine, haloperidol (haloperidol), loxapine (loxapine) and other drugs known to cause epileptic seizures

• In addition to the above items, patients who are deemed inappropriate by clinical trial researchers