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Table 1 Summary of the multicenter, double-blind, randomized placebo-controlled trials included in the base-case and sensitivity analyses.

From: Pregabalin versus gabapentin in partial epilepsy: a meta-analysis of dose-response relationships

Individual Studies

Pregabalin Trials

Daily Dose (Titration Period)

No. of Patients

Gabapentin Trials

Daily Dose (Titration Period)

No. of Patients

  

ITT

Completers

  

ITT

Completers

Beydoun et al 2005 [21] (Study 1008-009)

600 mg (1 week)

214

156

UK Gabapentin Study Group, 1990 [27] (Study 877-210P)

1200 mg (2 weeks)

61

54

 

Placebo

98

81

 

Placebo

66

61

Arroyo et al 2004 [20] (Study 1008-011)

150 mg (3 days)

99

88

The US Gabapentin Study Group No. 5, 1993 [26] (Study 945-5)d

1200 mg (2-3 days)

101

95

 

600 mg (1 week)

92

69

 

1800 mg (2-3 days)

54

53

 

Placebo

96

84

 

Placebo

98

96

French et al 2003 [23] (Study 1008-034)a,b

150 mg

86

81

Anhut et al 1994 [24] (Study 945-6)

900 mg (2 days)

109

100

 

300 mg

90

71

    
 

600 mg

89

61

 

1200 mg (2 days)

52

50

 

Placebo

100

87

 

Placebo

109

100

Elger et al 2005 [22] (Study 1008-157)b,c

600 mg

137

80

Sivenius et al 1991 [25] (Study 945-9/10)

900 mg (2 days)

36

32

     

1200 mg (2 days)

17

16

 

Placebo

73

56

 

Placebo

34

30

Aggregated Studies

Treatment in Pregabalin Trials

Daily Dose

No. of Patients

Treatment in Gabapentin Trials

Daily Dose

No. of Patients

  

ITT

Completers

  

ITT

Completers

Placebo

 

367

308

Placebo

 

307

287

Low-Dose Pregabalin

150 mg

185

169

Low-Dose Gabapentin

900 mg

145

132

Mid-Dose Pregabalin

300 mg

90

71

Mid-Dose Gabapentin

1200 mg

231

215

High-Dose Pregabalin

600 mg

532

366

High-Dose Gabapentin

1800 mg

54

53

  1. All studies had a 12-week double-blind maintenance phase but the durations of the titration phases were variable.
  2. aIn addition to the doses listed above, for trial 1008-034 patients were also recruited into a 50 mg dose group. This dose was not found to be therapeutic and is not registered for use in Australia.
  3. bNo titration phase.
  4. cIn addition to the doses listed above, for trial 1008-157 patients were also recruited into a titrated dose arm with total daily doses ranging from 150 mg to 600 mg, depending on individual requirement. This treatment group was not comparable with the other fixed-dose treatment groups and was excluded from the analyses.
  5. dIn addition to the doses listed above, for trial 945-5 patients were also recruited into a 600 mg dose group. This dose was not found to be therapeutic and is not registered in Australia.
  6. ITT = intention-to-treat.