Abstract |
Gabapentin (GBP) has been shown to be effective an add-on drug for the treatment of refractory partial epilepsy. We undertook an open clinical trial to test its efficacy for the first time in India. Twenty-six patients with refractory partial seizures (> 4 per month) were given GBP in a titrated dose and the seizure frequency was noted for 3 months. The mean reduction in seizures was significant: 15.87 (SD = 4.5) vs 5.80 (SD = 10.25). The mean percentage change (PCH) from the baseline was -36. Twenty-one of 26 (80%) patients had a reduction in the number of seizures, and 13/26 (50%) were identified as responders (> 50% reduction in seizures). The responders were significantly younger than the nonresponders. Adverse events were mild and noted in 46% patients. Although the trial has its limitations, this is probably the first trial of GBP in a developing country.
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Authors | S N Dixit, S Jain, M V Padma, M C Maheshwari |
Journal | Acta neurologica Scandinavica
(Acta Neurol Scand)
1996 Feb-Mar
Vol. 93
Issue 2-3
Pg. 85-7
ISSN: 0001-6314 [Print] Denmark |
PMID | 8741123
(Publication Type: Clinical Trial, Journal Article)
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Chemical References |
- Acetates
- Amines
- Anticonvulsants
- Cyclohexanecarboxylic Acids
- gamma-Aminobutyric Acid
- Gabapentin
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Topics |
- Acetates
(adverse effects, therapeutic use)
- Adolescent
- Adult
- Amines
- Anticonvulsants
(adverse effects, therapeutic use)
- Cyclohexanecarboxylic Acids
- Developing Countries
- Drug Therapy, Combination
- Electroencephalography
(drug effects)
- Epilepsies, Partial
(drug therapy)
- Female
- Gabapentin
- Humans
- India
- Male
- Middle Aged
- Treatment Outcome
- gamma-Aminobutyric Acid
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