Not Yet RecruitingN/Aketamine
Esketamine Combined With PRF for Trigeminal Postherpetic Neuralgia
Sponsored by Beijing Tiantan Hospital
NCT ID
NCT06914180
Target Enrollment
174 participants
Start Date
2025-04-01
Est. Completion
2026-07-01
About This Study
This trial's primary objective is to compare the analgesic efficacy of esketamine in combination with pulsed radiofrequency (PRF) against that of PRF monotherapy in patients with trigeminal postherpetic neuralgia (TPHN).
Conditions Studied
Interventions
- •esketamine group
- •control group
Eligibility
Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: 1. Ages more than 18 years; 2. Pain persisting for over three months following the onset of the herpes zoster skin rash; 3. Lesions located in the trigeminal nerve or its branches innervated regions; 4. Having an average pain score of at least 4 on a Numeric Rating Scale (NRS, 0 = no pain, 10= worst possible pain); 5. Planned to perform CT-guided PRF treatment of the gasserian ganglion(GG). Exclusion Criteria: 1. Obstructive sleep apnoea syndrome; 2. Those who receive other more invasive treatments, such as radiofrequency thermocoagulation (RFT) of GG. 3. A history of systemic immune diseases, organ transplantation, or cancers; 4. A history of severe cardiopulmonary, hepatic, renal dysfunction or coagulation function disorder; 5. A history of schizophrenia, epilepsy, or myasthenia gravis, delirium; 6. Comorbid hyperthyroidism or phaeochromocytoma; 7. Recent history of drug abuse; 8. Having contraindications to esketamine; 9. Communication difficulties. 10. Women who are preparing for pregnancy, in the pregnancy or lactation period.
Study Locations (1)
Beijing Tiantan Hospital
Beijing, Beijing Municipality, China