Efficacy of L/A Spray andL/A-soaked Nasal Packings on Postoperative Pain After Nasal Closed Reduction
- Registration Number
- NCT03733275
- Lead Sponsor
- The Catholic University of Korea
- Brief Summary
This study is perfored to investigate the efficacy of preoperative lidocaine spray and lidocaine-bupivacaine mixture-soaked nasal packing for acute postoperative pain after nasal closed reduction surgery.
- Detailed Description
To investigate the treatment of postoperative pain after nasal closed reduction surgery, we plan to investigate the effect of preoperative lidocaine spray and lidocaine-bupivacaine mixture-soaked nasal packing for the patinets undergoing nasal closed reduction under general aensthesia, compaing to the control group (normal saline spray and normal saline-soaked nasal packing).
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 33
Inclusion Criteria
- patients scheduled to receive nasal reduction surgery under general aensthesia
Exclusion Criteria
- concomitant disorders (eg. facial bone fractures) concomitant surgery (eg. septoplasty)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description local anesthetic group Lidocaine local aensthetic group receive preopetaive lidocaine spray and lidocaine-bupivacine mixture-soaked nasal pacing after nasal reduction surgery control group Lidocaine control group receive preoperative normal saline spray and normal saline-soaked nasal packing after nasal reduction surgery
- Primary Outcome Measures
Name Time Method postoperative pain in recovery room immediately after surgery Using VAS, postoperative pain is measured.
- Secondary Outcome Measures
Name Time Method rescue analgesics in recovery room 1 hr after surgery Fentanyl iv injection for pain control is checked.
Trial Locations
- Locations (1)
Seoul St.Mary's Hospital
🇰🇷Seoul, Seocho-gu, Korea, Republic of
Seoul St.Mary's Hospital🇰🇷Seoul, Seocho-gu, Korea, Republic of