The application of focused solution mode in CT guided percutaneous radiofrequency thermocoagulation of stem and breast foramen for the treatment of fear of pain in patients with facial spasm

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300067881

Enrollment

Unknown

Registered

2023-01-30

Start date

2023-02-01

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

Hemifacial spasm

Interventions

experience group:SFA nursing intervention model

Control group:Routine nursing intervention mode

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Conform to the diagnostic criteria of facial spasm; 2. Aged >= 18 years; 3. The patients who agreed to perform percutaneous radiofrequency thermocoagulation of the stem and breast foramen under CT guidance; 4. Conscious and able to cooperate with the researcher.

Exclusion criteria

Exclusion criteria: Exclusion and exclusion criteria: 1. Patients with severe heart, brain, lung, liver, kidney dysfunction or autoimmune related diseases; 2. Severe cognitive impairment and language impairment; 3. People with mental illness; 4. Local infection or systemic infection at puncture site; 5. Thrombocytopenia or coagulation dysfunction; 6. Those who refuse to participate or ask to withdraw halfway.

Design outcomes

Primary

Measure	Time frame
The Fear of Pain Questionnaire, FPQ;	—

Secondary

Measure	Time frame
visual analog scal;Social impact score;Accuracy of bulge cheek movement;	—

Countries

China

Contacts

Public ContactXia Jianmei

The First Hospital Jiaxing

676912880@qq.com+86 13957392629

Outcome results

None listed

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