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

Orofacial Pain

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

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source

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