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A clinical study of hemodynamic stability of percutaneous compression of the trigeminal ganglion for trigeminal neuralgia

A clinical cohort study of hemodynamic stability of percutaneous compression of the trigeminal ganglion for trigeminal neuralgia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017699
Enrollment
Unknown
Registered
2018-08-10
Start date
2018-08-10
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

Trigeminal neuralgia

Interventions

groupA:saline
groupB:sodium nitroprusside
groupC:atropine
group D: Remifentanil
groupE:propofol

Sponsors

Liaoning people's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients who had agreed to be experimented after informed clinical observation; patients with primary trigeminal neuralgia, non secondary trigeminal neuralgia (such as intracranial tumor occupying), and normal cardiopulmonary function.

Exclusion criteria

Exclusion criteria: Patients with bradycardia (<50bpm); psychic or neurologic diseases; serious heart, lung, brain and kidney diseases; patients with allergic drug use; foreign patients; illiterate, language difficult to communicate, and uncooperative patients.

Design outcomes

Primary

MeasureTime frame
heart rate;—

Secondary

MeasureTime frame
Systolic Blood Pressure,SBP;Diastolic Blood Pressure;Cardiac Output;SVV;Heart Rate Variation;System Vascular Resistance;Bispectral Idex;cerebral regional oxygen saturation;—

Countries

China

Contacts

Public ContactChang-Ming Wang

Liaoning people's Hospital

wchangming@163.com+86 17702486100

Outcome results

None listed

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