Table 3.
Clinical Trial | Ref. | LA Dose administered to human subjects | Subjects receiving LA |
Parameters measured† |
---|---|---|---|---|
Diabetes: ALADIN |
[37] | 100, 600, or 1200 mg, intravenous for 3 weeks | 328 | Neuropathic symptoms, HPAL, NDS |
Diabetes: ALADIN II |
[38] | a) 600 mg, intravenous, for 5 days + 600 mg, orally for 2 years b) 1200 mg, intravenous for 5 days + 1200 mg, orally for 2 years |
a) 27 b) 18 |
NDS, electrophysiological attributes of the sural and tibial nerves |
Diabetes: ALADIN III |
[39] | a) 600 mg, intravenous, for 3 weeks + 1800 mg (600 mg t.i.d.) for 6 months b) 600 mg, intravenous, for 3 weeks + placebo for 6 months |
a) 165 b) 173 |
TSS, NIS |
Diabetes | [40] | a) 600 mg, oral, for 4 weeks b) 1200 mg (600 mg b.i.d.), orally for 4 weeks c) 1800 mg (600 mg t.i.d.), orally for 4 weeks |
a) 19 b) 18 c) 18 |
Insulin-stimulated glucose disposal |
Diabetes: ORPIL |
[41] | 1800 mg (600 mg t.i.d.), orally for 3 weeks | 12 | TSS, HPAL, NDS |
Diabetes: SYDNEY |
[42] | 600 mg, intravenous, 5 days a week for 14 treatments | 60 | NCS, TSS, NIS, quantitative sensation test, autonomic test |
Diabetes: SYDNEY II |
[43] | a) 600 mg, orally for 5 weeks b) 1200 mg, orally for 5 weeks c) 1800 mg, orally for 5 weeks |
a) 45 b) 47 c) 46 |
TSS, NCS, NIS |
Diabetes: DEKAN |
[44] | 800 mg (200 mg q.i.d.), orally for 4 months | 39 | Cardiac autonomic nerve function |
Diabetes | [45] | 600 mg/day, orally for 3 months | 33 | Plasma lipid hydroperoxides, alpha-tocopherol, cholesterol |
Multiple Sclerosis |
[46] | a) 1200 mg q.d. b) 1200 mg (600 mg b.i.d.) c) 2400 mg (1200 mg b.i.d.) |
a) 9 b) 7 b) 7 |
Serum LA, Matrix Metalloproteinase-9, and Intercellular Adhesion Molecule-1 |
Metabolic Syndrome: ISLAND |
[47] | 300 mg, orally for 4 weeks | 15 | Endothelial function and proinflammatory markers |
HPAL = Hamburg Pain Adjective List, NDS = Neuropathy Disability Score, NIS = Neuropathy Impairment Score, NSC = Neuropathic Symptoms and Change Score, TSS = Total Symptom Score