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Clinical Trials in China / NCT06890897
Recruiting Not applicable

Esketamine Combined Pulsed Radiofrequency for Acute/Subacute Zoster-associated Trigeminal Neuralgia

NCT06890897 · tracked via the Priya Life Science China tracker
Sponsor
Beijing Tiantan Hospital
Phase
Not applicable
Started
2025-04-01
Last updated
2025-04-27

Condition(s) studied

Zoster; Herpes, Trigeminal Neuralgia (Etiology)

Investigational drug(s) / intervention(s)

Esketamine groupPRF group

Esketamine group: Patients in the esketamine group will receive intravenous infusion of esketamine besides PRF+standardized treatment.The formula will be intravenous infusion of 0.5mg/kg of esketamine diluted in 50 mL normal saline, starting with intravenous injection of 10 mg of esketamine for 1 minute, and maintaining a dose 8 mg/h.The infusion rate will be adjusted the parameter according to the tolerance of the patients

PRF group: Patients in the control group will receive PRF+standardized treatment

Study summary

To assess the 1-month effects and safety of esketamine combined PRF and standardized treatment to relieve pain in patients with acute/subacute zoster-related trigeminal neuralgia(ZRTN).

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Age \>18 years; 2. History of HZ within the last three months; 3. Lesions located in the trigeminal nerve or its branches innervated regions; 4. Numeric Rating Scale (NRS) pain score≥4 (NRS, 0 = no pain, 10= worst possible pain) with pharmacotherapy; 5. Planned to perform CT-guided PRF treatment of the Gasserian ganglion . Exclusion Criteria: 1. Obstructive sleep apnoea syndrome; 2. Those who receive other invasive treatments, such as spinal cord stimulation; 3. A history of systemic immune diseases, organ transplantation, or cancers; 4. A history of severe cardiopulmonary, hepatic or renal dysfunction; 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. Withdrawal criteria 1. Lost to follow-up during the study; 2. Not perform the planned operation; 3. Receiving other treatment regimes during the study period; 4. Not suitable for continuing the study for emerging severe comorbidities or special physiological changes during the study; 5. Voluntary withdrawal from the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beijing Tiantan Hospital Beijing China Recruiting

More Beijing Tiantan Hospital trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06890897 on ClinicalTrials.gov ↗ ← All trials in China