Esketamine Combined With PRF for Trigeminal Postherpetic Neuralgia

NANot yet recruitingINTERVENTIONAL
Enrollment

174

Participants

Timeline

Start Date

April 1, 2025

Primary Completion Date

April 1, 2026

Study Completion Date

July 1, 2026

Conditions
Postherpetic; Neuralgia, Trigeminal (Etiology)
Interventions
DRUG

esketamine group

In the esketamine group, in addition to receiving PRF treatment+pregabalin for rescue analgesia, patients will also undergo a single intravenous infusion of esketamine. A total of 0.5 mg/kg of esketamine will be diluted in 50 mL of normal saline. The infusion will commence with an intravenous injection of 10 mg of esketamine over 1 minute, followed by a maintenance dose of 8 mg/h. The infusion rate will be adjusted based on the patients' tolerance levels.

DRUG

control group

In the control group, patients will receive PRF+pregabaline treatment. Pulsed radiofrequency (PRF) will be performed on GG by a designated physician in each participating center. PRF treatment (PMG-230, Baylis Medical Inc.) targeting to GG will be applied for 900 seconds. The parameters of PRF treatment will be set at 42 ℃, 2 Hz with 20 milliseconds current. Regarding pregabalin, the dosage is titrated based on patients'pain intensity and tolerance. This process fully accounts for individual patient differences to optimize treatment outcomes.

Trial Locations (1)

100070

Beijing Tiantan Hospital, Beijing

All Listed Sponsors
collaborator

Beijing Xiaotangshan Hospital

OTHER

collaborator

The First Hospital of Fangshan District,Beijing

OTHER

collaborator

Beijing Ditan Hospital

OTHER

collaborator

Hengshui People's Hospital

OTHER

lead

Beijing Tiantan Hospital

OTHER

NCT06914180 - Esketamine Combined With PRF for Trigeminal Postherpetic Neuralgia | Biotech Hunter | Biotech Hunter