Not Yet RecruitingPhase 2ketamine
Safety and Efficacy of Lidocaine Versus Ketamine Infusion for Resistant Orofacial Pain
Sponsored by Assiut University
NCT ID
NCT07250867
Target Enrollment
105 participants
Start Date
2026-01
Est. Completion
2027-02
About This Study
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.
Conditions Studied
Interventions
- •Lidocaine Intravenous Infusion
- •Ketamine intravenous infusion
- •Combined lidocaine and ketamine intravenous infusion
Eligibility
Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: \- Adults aged \> 18 years Resistant orofacial pain patients with failed medical or interventional treatment Diagnosed with one or more of the following: Trigeminal neuralgia Temporomandibular joint (TMJ) dysfunction Malignant otitis externa Migraine Atypical facial pain Exclusion Criteria: \- Debilitating cardiac disease Uncontrolled hypertension Known allergies to lidocaine or ketamine Severe renal or hepatic impairment Pregnancy or breastfeeding History of substance abuse