Long Term Outcome After Serial Lidocaine Infusion in Peripheral Neuropathic Pain

Last updated: November 24, 2022
Sponsor: Mahidol University
Overall Status: Completed

Phase

3

Condition

Peripheral Neuropathy

Pain

Pain (Pediatric)

Treatment

N/A

Clinical Study ID

NCT02217267
SI140/2014
  • Ages 18-75
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The purpose of this study to evaluated Long term outcome after serial Lidocaine infusion when compared with placebo in peripheral neuropathic pain patients in acute stage (less than 6 months) at 3 months after first time of infusion

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Peripheral neuropathic pain from peripheral nerve injury within 6 months after injury
  • Well understand to Thai language in writing or listening

Exclusion

Exclusion Criteria:

  • Underlying Heart disease or Arrhythmia
  • Allergy to lidocaine, Gabapentin, Carbamazepine, tramadol
  • History of epilepsy
  • History of lidocaine used
  • Underlying Psychiatric disease
  • History of drug abuse
  • Pregnancy and nursing

Study Design

Total Participants: 29
Study Start date:
August 01, 2014
Estimated Completion Date:
February 28, 2018

Study Description

Peripheral nerve injury may give rise to severe and long-lasting types of pains which are often resistant to treatment such as opioid, tricyclic antidepressant or anticonvulsant. Lidocaine infusion has been the one of intractable neuropathic pain treatment . My hypothesis the serial lidocaine infusion can adequate pain control and can prevent chronic pain (central sensitisation). Therefore, we designed this prospective, randomised, double-blind, controlled study to evaluate the efficacy of serial lidocaine infusion in peripheral neuropathic pain compared with placebo in long term outcome (at 3 month).

Connect with a study center

  • Faculty of medicine Siriraj Hospital Mahidol University

    Bangkoknoi, Bangkok 10700
    Thailand

    Site Not Available

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