Trigeminal neuralgia
Conditions
Interventions
Observational group:None
Sponsors
The First Affiliated Hospital of Army Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Age >= 18 years; 2. Diagnosed with trigeminal neuralgia according to the diagnostic criteria of the International Headache Society; 3. Patients scheduled to undergo operative treatments such as microvascular decompression (MVD), percutaneous balloon compression (PBC), radiofrequency ablation, nerve block, or gamma knife; 4. Provided informed consent and voluntarily participated in this study; 5. Alert and able to express intentions clearly.
Exclusion criteria
Exclusion criteria: 1. Coexisting severe somatic diseases or severe cognitive impairment (e.g., heart failure, stroke) affecting daily living, with hospitalization within the past six months; 2. History of psychiatric disorders (e.g., depression, anxiety); 3. Individuals with drug or alcohol dependence, or those who have experienced a major life event recently; 4. Severe cardiac, hepatic, or renal insufficiency; 5. Pregnant or breastfeeding women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Chinese version memorial symptom assessment Scale, MSAS-Ch;Symptom occurrence at different time points perioperatively in patients with trigeminal neuralgia (incidence, frequency, severity, distress level, symptom score);Number, types, and composition of symptom clusters at different time points perioperatively in patients with trigeminal neuralgia;Core symptoms of symptom clusters at different time points perioperatively in patients with trigeminal neuralgia; | — |
Secondary
| Measure | Time frame |
|---|---|
| General information questionnaire (including gender, age, occupation, etc.); | — |
Countries
China
Contacts
Public ContactXian Jishu
The First Affiliated Hospital of Army Medical University
Outcome results
None listed