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Table 2 Audiometric and psychoacoustic characteristics of patients at screening (ITT population)

From: A randomized, double-blind, placebo-controlled clinical trial to evaluate the efficacy and safety of neramexane in patients with moderate to severe subjective tinnitus

 

N

Mean ± SD

Puretone audiometry (worst ear)

Hearing threshold [dB]

  

   Placebo

111

19.9 ± 10.6

   Neramexane 25 mg/d

106

20.1 ± 12.6

   Neramexane 50 mg/d

106

19.4 ± 10.6

   Neramexane 75 mg/d

99

20.6 ± 14.7

High frequency hearing threshold [dB]

  

   Placebo

111

36.9 ± 20.2

   Neramexane 25 mg/d

106

36.0 ± 21.4

   Neramexane 50 mg/d

106

36.6 ± 21.7

   Neramexane 75 mg/d

99

36.9 ± 19.9

Tinnitus matching (worst ear)

Frequency (pitch) match [Hz]

  

   Placebo

109

4577.5 ± 2601.9

   Neramexane 25 mg/d

105

4915.1 ± 2596.2

   Neramexane 50 mg/d

103

4958.7 ± 2683.1

   Neramexane 75 mg/d

97

4920.9 ± 2804.8

Loudness match [dB]

  

   Placebo

105

38.6 ± 19.3

   Neramexane 25 mg/d

103

40.5 ± 20.5

   Neramexane 50 mg/d

99

39.3 ± 20.3

   Neramexane 75 mg/d

91

39.2 ± 18.5

Minimal masking level (worst ear)

Masking level [dB]

  

   Placebo

106

44.8 ± 21.0

   Neramexane 25 mg/d

100

46.8 ± 19.0

   Neramexane 50 mg/d

99

44.8 ± 21.1

   Neramexane 75 mg/d

92

44.2 ± 20.6

  1. ITT = intent-to-treat, N = number of patients, SD = standard deviation