Correlation research for clinical results with the balloon shape, the pressure, the compression time during percutaneous balloon compression for patients with trigeminal neuralgia

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1900025678

Enrollment

Unknown

Registered

2019-09-05

Start date

2019-10-01

Completion date

Unknown

Last updated

2020-10-13

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

Conditions

raise independently

Interventions

single arm:Treatment of Balloon Compressors

Eligibility

Sex/Gender

All

Age

20 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Primary trigeminal neuralgia patients; 2. Patients who are ineffective or unable to tolerate side effects of drugs; 3. Patients who are unable, unsuitable or unwilling to undergo microvascular decompression and willing to undergo balloon compression therapy.

Exclusion criteria

Exclusion criteria: 1. Patients with secondary trigeminal neuralgia, and who are not suitable for trigeminal nerve balloon compression therapy; 2. Patients with trigeminal nerve lesions such as superficial hypoesthesia and masticatory muscle weakness before balloon compression; 3. Patients who are unwilling to be observed.

Design outcomes

Primary

Measure	Time frame
Balloon working pressure;Balloon compression time;balloon shape;VAS score of preoperative pain;VAS score of postoperation pain;	—

Secondary

Measure	Time frame
Postoperative tinnitus;	—

Countries

China

Contacts

Public ContactZhou Le

Department of Neurosurgery, the Second Affiliated Hospital of Xi'an Jiaotong University

drzhoule@163.com+86 15009265580

Outcome results

None listed

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