CClinicalTrials.gg
TerminatedNCT00189072Updated Sep 16, 2005

Effects of Gabapentin in the Treatment of Neuropathic Pain on Driving Performance and Cognition

A Phase 4 interventional study of gabapentin in Chronic Neuropathic Pain, sponsored by UMC Utrecht. Terminated at 1 site in Netherlands. Open to participants aged 30 Years to 60 Years. Per ClinicalTrials.gov, last updated 2005-09-16.

Sponsored by UMC Utrecht · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
30 Years to 60 Years
Sex
All
01

Study summary

The aim of this study was to explore the effects of pain on the one hand and the effects of treatment of pain with gabapentin (900, 1200, 1800 or 2400 mg) on the other hand on actual driving performance and several laboratory tests in patients with neuropathic pain. It was hypothesized that gabapentin might influence performance after acute but not after subchronic administration.

Read the detailed description

Numerous studies demonstrate neuropsychological impairment in patients with chronic pain, particularely on measures assessing attentional capacity, processing speed and psychomotor speed. About 50% of the patients suffering from neuropathic pain are treated with anticonvulsants, as a treatment against serious pain complaints, and experience good pain relief. Gabapentin is one of the most prescribed anticonvulsants for the treatment of neuropathic pain. An important disadvantage of treatment with gabapentin could be the occurrence of side effects, such as somnolence and fatigue. These side effects can constitute a crucial problem for patients treated with gabapentin who must operate a motor vehicle or other dangerous machinery. However, pain affects cognition negatively, and possibly also driving. Therefore, another possibility is that treatment with gabapentin for these pain complaints can improve driving because the pain has less influence. Since driving is an activity of daily living that is important in maintaining independency in the community, such as access to employment and social activities, it is important to establish the effects of using gabapentin on these abilities. No studies have been conducted so far to investigate driving abilities of patients with neuropathic pain, treated with gabapentin.The aim of this study was to explore the effects of pain on the one hand and the effects of acute (Day 1) and subchronic (Day 15) treatment of pain with gabapentin (900, 1200, 1800 or 2400 mg) on the other hand on actual driving performance and several laboratory tests in patients with neuropathic pain. It was hypothesized that gabapentin might influence performance after acute but not after subchronic administration. This study is a two-period double-blind, placebo-controlled, cross-over randomised study.

02

Conditions studied

  • Chronic Neuropathic Pain

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Keywords

  • gabapentin
  • neuropathic pain
  • driving
  • attention
03

In context

Neuralgia

1,287 studies on the registry are indexed under Neuralgia; 256 are open to participants now.

This study's enrollment of 24 is below the median of 52 across 973 interventional studies indexed under Neuralgia.

Browse Neuralgia studies →

Lead sponsor

UMC Utrecht is the lead sponsor of 350 studies on the registry; 80 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • age, responder to gabapentin,succesfully treated with gabapentin at least 4 weeks before start of study, minimal VAS pain intensity scores of 4 cm on a 10 cm scale, driving licence, driving experience, fluently speaking Dutch, normal vision, right-handed

Exclusion criteria

Exclusion Criteria:

  • alcohol- or drug dependence, use of other psychotropic medication, use of illicit drugs, psychological or physical disorder other than pain or pain-related, excessive smoking and drinking
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double
Enrollment
24 participants

Interventions

  • Druggabapentin
06

What researchers measure

Primary outcomes

  1. driving test parameters

Secondary outcomes

  1. laboratory test parameters

  2. Event Related Potentials

07

Study locations

1 site
  • University of Utrecht
    Utrecht, 3508 TB, Netherlands
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 16, 2005, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00189072
Lead sponsor
UMC Utrecht
Collaborators
Utrecht University
First posted
Sep 16, 2005
Start date
Apr 2003
Last update
Sep 16, 2005

Study contacts

Edmund Volkerts, PhD
principal investigator · Utrecht University
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in May 2005. You cannot join it, but the record below documents what was studied.

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