Effect of compression pressure and compression time on the prognosis of primary trigeminal neuralgia treated with balloon compression

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200061078

Enrollment

Unknown

Registered

2022-06-15

Start date

2022-06-01

Completion date

Unknown

Last updated

2023-03-26

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

Conditions

Trigeminal Neuralgia

Interventions

No:No

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients with primary trigeminal neuralgia; 2. Those who are ineffective or intolerable to drug treatment; 3. Those who are unsuitable or unwilling to accept microvascular decompression for treatment and agree to accept percutaneous balloon compression for treatment; 4. Sign the informed consent; 5. Consent to data collection and follow-up observation.

Exclusion criteria

Exclusion criteria: 1. Patients who are unsuitable or unwilling to undergo percutaneous balloon compression surgery; 2. Patients with facial nerve numbness and other symptoms before balloon compression surgery, which may interfere with the judgment of the effect of surgical treatment; 3. TN patients Complications of puncture site infection, severe cardiopulmonary insufficiency, and coagulation dysfunction; 4. Those who do not have the ability to act autonomously.

Design outcomes

Primary

Measure	Time frame
Compression time;Compression pressure;	—

Countries

China

Contacts

Public ContactZhou Bo

Graduate School of China Medical Univerrsity

ripple_zhou@126.com+86 13709826820

Outcome results

None listed

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