Next-day residual effects of gabapentin, diphenhydramine, and triazolam on simulated driving performance in healthy volunteers: a phase 3, randomized, double-blind, placebo-controlled, crossover trial.

Gary G Kay, Howard I Schwartz, Mark A Wingertzahn, Shyamalie Jayawardena, Russell P Rosenberg
Author Information
  1. Gary G Kay: Cognitive Research Corporation, St. Petersburg, Florida, USA.
  2. Howard I Schwartz: Miami Research Associates, South Miami, Florida, USA.
  3. Mark A Wingertzahn: Pfizer Consumer Healthcare, Madison, New Jersey, USA.
  4. Shyamalie Jayawardena: Pfizer Consumer Healthcare, Madison, New Jersey, USA.
  5. Russell P Rosenberg: Neurotrials Research Inc., Atlanta, Georgia, USA.

Abstract

OBJECTIVE: Next-day residual effects of a nighttime dose of gabapentin 250 mg were evaluated on simulated driving performance in healthy participants in a randomized, placebo-controlled, double-blind, multicenter, four-period crossover study that included diphenhydramine citrate 76 mg and triazolam 0.5 mg.
METHODS: At treatment visits, participants (n = 59) were dosed at ~23:30, went to bed immediately, and awakened 6.5 h postdose for evaluation. The primary endpoint was the standard deviation of lateral position for the 100-km driving scenario. Additional measures of driving, sleepiness, and cognition were included.
RESULTS: Study sensitivity was established with triazolam, which demonstrated significant next-day impairment on all driving endpoints, relative to placebo (p < 0.001). Gabapentin demonstrated noninferiority to placebo on standard deviation of lateral position and speed deviation but not for lane excursions. Diphenhydramine citrate demonstrated significant impairment relative to gabapentin and placebo on speed deviation (p < 0.05). Other comparisons were either nonsignificant or statistically ineligible per planned, sequential comparisons. Secondary endpoints for sleepiness and cognitive performance were supportive of these conclusions.
CONCLUSIONS: Together, these data suggest that low-dose gabapentin had no appreciable next-day effects on simulated driving performance or cognitive functioning. Copyright © 2016 John Wiley & Sons, Ltd.

Keywords

MeSH Term

Adult
Amines
Analgesics
Anti-Anxiety Agents
Automobile Driving
Cognition
Cross-Over Studies
Cyclohexanecarboxylic Acids
Diphenhydramine
Double-Blind Method
Female
Gabapentin
Humans
Hypnotics and Sedatives
Male
Middle Aged
Sleep Stages
Time Factors
Triazolam
gamma-Aminobutyric Acid

Chemicals

Amines
Analgesics
Anti-Anxiety Agents
Cyclohexanecarboxylic Acids
Hypnotics and Sedatives
Triazolam
gamma-Aminobutyric Acid
Gabapentin
Diphenhydramine

Word Cloud

Created with Highcharts 10.0.0drivinggabapentinperformanceeffectssimulateddeviationresidualdiphenhydraminetriazolamdemonstratedplaceboNext-dayhealthyparticipantsrandomizedplacebo-controlleddouble-blindcrossoverincludedcitratestandardlateralpositionsleepinesssignificantnext-dayimpairmentendpointsrelativep < 0speedcomparisonscognitiveOBJECTIVE:nighttimedose250 mgevaluatedmulticenterfour-periodstudy76 mg05 mgMETHODS:treatmentvisitsn = 59dosed~23:30wentbedimmediatelyawakened65 hpostdoseevaluationprimaryendpoint100-kmscenarioAdditionalmeasurescognitionRESULTS:Studysensitivityestablished001GabapentinnoninferioritylaneexcursionsDiphenhydramine05eithernonsignificantstatisticallyineligibleperplannedsequentialSecondarysupportiveconclusionsCONCLUSIONS:Togetherdatasuggestlow-doseappreciablefunctioningCopyright©2016JohnWiley&SonsLtdvolunteers:phase3trialsleep

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