Nasal Fracture
Conditions
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).
Interventions
DRUGLidocaine
for experimental arm, lidocaine spray and lidocaine bupivacine mixture-soaked nasal packing vs. for placebo arm, normal saline spray and packing
Sponsors
The Catholic University of Korea
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
* patients scheduled to receive nasal reduction surgery under general aensthesia
Exclusion criteria
* concomitant disorders (eg. facial bone fractures) concomitant surgery (eg. septoplasty)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| postoperative pain in recovery room | immediately after surgery | Using VAS, postoperative pain is measured. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| rescue analgesics in recovery room | 1 hr after surgery | Fentanyl iv injection for pain control is checked. |
Countries
South Korea
Outcome results
None listed