FindTrial
Sign In

Individualized balloon volume in percutaneous balloon compression for trigeminal neuralgia

Analysis of individualized balloon volumes based on Meckel's cave size measured by MRI in the prognosis of percutaneous balloon compression for trigeminal neuralgia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200056114
Enrollment
Unknown
Registered
2022-02-01
Start date
2022-01-24
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Trigeminal neuralgia

Interventions

Observation group :None

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. A clear diagnosis of trigeminal neuralgia; 2. Complete clinical data retention; 3. Age of patient >= 18 years; 4. No other comorbid chronic headache disorder such as migraine or tension-type headache; 5. A pear-shaped balloon; 6. The compression duration is 180 s.

Exclusion criteria

Exclusion criteria: 1. Secondary trigeminal neuralgia; 2. Mental disability or psychiatric disorder; 3. Having undergone another surgical intervention such as MVD or radiofrequency (RF); 4. Patients who refused to participate in the study.

Design outcomes

Primary

MeasureTime frame
balloon volume;—

Countries

China

Contacts

Public ContactXiaochong Fan

The First Affiliated Hospital of Zhengzhou University

fccfxc@zzu.edu.cn+86 13513807717

Outcome results

None listed

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