Trigeminal neuralgia
Conditions
Interventions
Observation Group (Phase I):Without intervention, imaging data—including cranial base CT and MRI—and electronic health records were collected from 110 patients with trigeminal neuralgia. These multimo
Trial group:The balloon compression procedure of the trigeminal ganglion was performed using a patient-specific 3D-printed navigation template
Sponsors
Xuanwu Hospital Capital Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.Age 18–75; 2.No gender restrictions; 3.Pain VAS score >= 4; 4.Pain duration >= 3 months; 5.MRI imaging results indicate no tumors, hemorrhages, or other secondary causes. 6.Agreed to participate in the study and signed the informed consent form.
Exclusion criteria
Exclusion criteria: 1.Pregnant women or individuals with severe cardiovascular or cerebrovascular diseases; 2.Patients with suspected infection (clinical signs + laboratory tests) requiring immediate control; 3.Patients with intracranial tumors or other space-occupying lesions requiring prior surgery; 4.Patients with severe mental illnesses or other conditions that prevent them from cooperating;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Balloon Formation Rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient Satisfaction;Therapeutic Effect Evaluation;Pain Condition;A significant reduction (>=50%) in oral analgesic medication use;Baseline data;Balloon injection volume (ml);Balloon compression time (minutes);Masseter muscle function;Number of X-ray exposures;Reveal foramen ovale exposure time (minutes);Grades of Patent Foramen Ovale;Numbness Condition;Imaging examination; | — |
Countries
China
Contacts
Public ContactYang Liqiang
Xuanwu Hospital Capital Medical University
Outcome results
None listed