Effect of superficial cervical plexus block for pain control in transoral robotic thyroidectomy: a prospective randomized controlled trial
Not Applicable
- Conditions
- Neoplasms
- Registration Number
- KCT0006690
- Lead Sponsor
- Hanyang University Seoul Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
a. Patients aged 20 to 65 years undergoing trans-oral robotic thyroidectomy or conventional open thyroidectomy under general anesthesia.
b. Grade I or II of American Society of Anesthesiologist (ASA) physical status classification system
Exclusion Criteria
a. Patients who disagree with this study.
b. Patients with a history of increased intracranial pressure or central nervous system diseases such as a brain tumor
c. Past history of hypersensitivity or allergic reaction to local anesthetics
d. If extensive surgery is scheduled, such as cervical lymphadenectomy
e. If there is a deformation of the neck structure due to histories of neck surgery or inflammatory diseases
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method post-operative pain score
- Secondary Outcome Measures
Name Time Method Total dose of analgesic agents administered in the recovery room;perioperative vital signs (blood pressure, heart rate, oxygen saturation);vital sign(blood pressure, heart rate, saturation), nausea and vomiting, dizziness, and headache;total operation time, total anesthesia time, total recovery time;The amount of fluid administered and the amounts of urine and blood loss during surgery