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Clinical Study for Percutaneous Balloon Compression Kits

Clinical Study for Percutaneous Balloon Compression Kits

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024787
Enrollment
Unknown
Registered
2019-07-27
Start date
2019-10-01
Completion date
Unknown
Last updated
2019-07-29

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

Conditions

Primary Trigeminal Neuralgia

Interventions

Case series:Percutaneous Balloon Compression Kits

Sponsors

Liaoning Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Male and female patients aged 18 to 70 years old; 2. Patients with Primary Trigeminal Neuralgia; 3. VAS score is more than or equal to 5 (without medicine). Use CT/MRI examination to identify the Primary Trigeminal Neuralgia and intracranial disease.

Exclusion criteria

Exclusion criteria: 1. Severe visceral disease; 2. Patients with coagulation disorders; 3. Secondary trigeminal neuralgia; 4. Patients with general anesthesia intolerance; 5. Patients with Active infection (including otitis media, mastoiditis); 6. Women who refuse to use contraceptive method; 7. Gestation period or lactation period.

Design outcomes

Primary

MeasureTime frame
Pain Relief Rate post operation;—

Secondary

MeasureTime frame
Wound area;Amount of bleeding;Hospital Stay;time of operation;—

Countries

China

Contacts

Public ContactMa Yi

Liaoning Provincial People's Hospital

976429342@qq.com+86 13940205763

Outcome results

None listed

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