Tomovic 1999.
| Methods | Randomised, parallel‐group study in Serbia | |
| Participants | 9 women and 9 men with refractory focal epilepsy. Serbian adults. Mean age: 24.7 years, range 17‐47 years Drug‐resistant focal epilepsy All had been treated with 1 or 2 first‐line AEDs during 3 months before introducing gabapentin with unsatisfactorily controlled seizures Seizure frequency prior to treatment was unclear  | 
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| Interventions | Gabapentin 900 mg Gabapentin 1200 mg  | 
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| Outcomes | Seizure frequency Seizure freedom Haematological and biochemical analyses (4th and 12th week) and 24‐hour EEG on before therapy and on final week (week 12). Frequency of epileptiform discharges noted Reduction in seizure activity: 26%‐49%; 50‐99%; 100%; worse state Adverse effects  | 
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| Notes | 3 people did not complete the study and were not included in the study altogether (i.e. not included in demographics, etc.) | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement | 
| Random sequence generation (selection bias) | Unclear risk | Method of randomisation unclear | 
| Allocation concealment (selection bias) | Unclear risk | How participants allocated to each group unclear | 
| Blinding (performance bias and detection bias) All outcomes | Unclear risk | Unclear if tablets and packaging identical in appearance | 
| Incomplete outcome data (attrition bias) All outcomes | High risk | Unclear why 3 participants dropped out and excluded from analysis | 
| Selective reporting (reporting bias) | Low risk | Seizure frequency recorded; unclear how seizure activity measured. Otherwise standardised tests for both groups | 
| Other bias | Low risk | Study appeared free of other sources of bias |