Impact of cervical plexus block on inflammation response and early postoperative recovery in patients undergoing microvascular decompression

Impact of ultrasound-guided cervical plexus block on inflammation response and early postoperative recovery in trigeminal neuralgia or hemifacial spasm patients undergoing microvascular decompression

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0007629

Enrollment

Registered

2022-08-09

Start date

2022-09-01

Completion date

Unknown

Last updated

2022-09-20

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

Conditions

None listed

Interventions

Procedure/Surgery : For the experimental group, a cervical plexus block is conducted with 10 cc of 0.5% ropivacaine under ultrasound guidance. There will be no intervention for the control group.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients aged 20 to 79 with trigeminal neuralgia or hemifacial spasms undergoing microvascular decompression

Exclusion criteria

Exclusion criteria: Patients who do not agree to participate in the study Patients who show infection signs around the area where a cervical plexus block is planned Patients with a history of hypersensitivity to local anesthetics Patients with a history of craniotomy Patients who are on anticoagulant medication or have coagulation disorders Patients with psychiatric disorders such as dementia and delirium Patients who difficulty to answer QoR-15K

Design outcomes

Primary

Measure	Time frame
QoR-15K	—

Secondary

Measure	Time frame
Tumor necrosis factor-a;InterLeukin-6;InterLeukin-8;Hear rate;Mean blood pressure;Oxygen saturation;body temperature;white blood cell count;Red cell distribution width;Erythrocyte sedimentation rate;Segmented neutrophil;High sensitivity C-reactive protein;Fibrinogen;blood glucose;Operation time;Anesthesia time;Dose of propofol;Dose of remifentanil;Intraoperative event;Numerical Rating Scale for pain assessment;Postoperative administration of rescue analgesics;Postoperative nausea/vomiting;Postoperative administration of antiemetics;Length of hospital stay;Complications	—

Measure

Time frame

Tumor necrosis factor-a;InterLeukin-6;InterLeukin-8;Hear rate;Mean blood pressure;Oxygen saturation;body temperature;white blood cell count;Red cell distribution width;Erythrocyte sedimentation rate;Segmented neutrophil;High sensitivity C-reactive protein;Fibrinogen;blood glucose;Operation time;Anesthesia time;Dose of propofol;Dose of remifentanil;Intraoperative event;Numerical Rating Scale for pain assessment;Postoperative administration of rescue analgesics;Postoperative nausea/vomiting;Postoperative administration of antiemetics;Length of hospital stay;Complications

—

Countries

Korea, Republic of

Contacts

Public ContactKyung Won Shin

Seoul National University Hospital

skwskw1@naver.com+82-2-2072-2469

Outcome results