Efficacy and Safety of Lidocaine Infusion Treatment in Management of Neuropathic Pain (NCT02597257) | Clinical Trial Compass
UnknownPhase 2
Efficacy and Safety of Lidocaine Infusion Treatment in Management of Neuropathic Pain
South Korea44 participantsStarted 2015-08
Plain-language summary
The investigators conducted a randomized, Double blind, and Controlled Study to evaluate the Efficacy and safety of Lidocaine Infusion Treatment in Management of Neuropathic pain.
Who can participate
Age range20 Years – 80 Years
SexALL
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Inclusion Criteria:
* postherpetic neuralgia, diabetic polyneuropathy, peripheral neuropathy
* NRS score \> 4
* stable oral medication during the 1 month trial period
* volunteers with informed consent
Exclusion Criteria:
* pregnancy, breastfeeding, possibility of pregnancy
* pain from causes other than upper 3 indications
* hypersensitivity to lidocaine or other local anesthetics
* important disease of heart, kidney, liver or incurable disease that may affect the assessment of adverse effects, or may interfere with the completion of study
* severe conduction block
* history of other interventions that may affect the study
* Enrollment in other clinical trials within 30 days
* otherwise not suitable to study