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Clinical observation on the safety and efficacy of percutaneous microballoon compression for the treatment of primary trigeminal neuralgia

Clinical observation on the safety and efficacy of percutaneous microballoon compression for the treatment of primary trigeminal neuralgia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093782
Enrollment
Unknown
Registered
2024-12-11
Start date
2024-12-16
Completion date
Unknown
Last updated
2024-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary trigeminal neuralgia

Interventions

Observation group:None

Sponsors

Liaoning Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients with a clinical diagnosis of primary TN who received PBC treatment at the Liaoning Provincial People's Hospital from December 2024 to 2025 2.Enrolled patient age: 18 years =3 months, and lasts at least until 1 week before the investigation; 4.Able to communicate, willing to accept questionnaires and phone follow-ups.

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with secondary TN; 2.Patients unable to understand and respond to the questionnaire; 3.Patients with chronic debility and life-threatening illnesses or other forms of chronic pain; 4.Patients diagnosed with mental disorders before the first occurrence of TN; 5.Informed consent from the patient or their guardian could not be obtained.

Design outcomes

Primary

MeasureTime frame
Pain intensity scale score;

Secondary

MeasureTime frame
Visual analog scale score;Balloon volume;Balloon compression duration;Balloon pressure plateau value;Balloon pressure peak;Postoperative complications;Postoperative patients' satisfaction with the surgery;Hospital Anxiety and Depression Scale;

Countries

China

Contacts

Public ContactWang Changming

Liaoning Provincial People's Hospital

TeamWangCM@163.com+86 177 0248 6100

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026