At a glance
ClinicalIndex Comparison RecordN/ACompleted· 8 enrolled
Drug / intervention
Ultrasound-guided peripheral nerve block with 2% lidocainedrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
How "Central" is Central Post-stroke Pain? Investigating the Role of Peripheral Sensory Input in Maintaining Central Pain
In Brief
A clinical study evaluating Ultrasound-guided peripheral nerve block with 2% lidocaine for Central Post Stroke Pain. Completed, enrolled 8 participants across 1 site.
Detailed Summary
Prospective, open-label study in 10 patients with Central Post Stroke Pain (CPSP). The study will evaluate the effects of peripheral nerve blockade on spontaneous pain and evoked thermal and mechanical responses in CPSP, and assesses the associated local anesthetic pharmacokinetics.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCentral Post Stroke Pain
CountriesUnited States
CollaboratorsAarhus University Hospital
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedMay 2014
Enrollment StartAug 2014
Primary CompletionDec 2016
Study CompletionJan 2017
TodayJul 2026
First PostedMay 28, 2014
Enrollment StartAug 1, 2014
Primary CompletionDec 15, 2016
Study CompletionJan 25, 2017
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 12.1 years ago
Interventions
Ultrasound-guided peripheral nerve block with 2% lidocainedrug
Patients will have a peripheral nerve blockade with a local anesthetic (lidocaine) Assessment of spontaneous and evoked pain responses Completion of NPSI questionnaire Mapping of the affected limb