Safety and Efficacy of Lidocaine Versus Ketamine Infusion for Resistant Orofacial Pain

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorAssiut University

About this trial

A prospective, randomized, double-blind clinical trial comparing the safety and efficacy of intravenous lidocaine, ketamine, and their combination as treatment options for patients suffering from treatment-resistant orofacial pain. The study measures pain reduction primarily using the Visual Analog Scale and evaluates safety and tolerability over a follow-up period of 6 months.

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Lidocaine Intravenous Infusion
  • Ketamine intravenous infusion
  • Combined lidocaine and ketamine intravenous infusion

Treatment groups

105 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators