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Clinical Trials/NCT03733275
NCT03733275CompletedNot Applicable

Efficacy of Preoperative Lidocaine Spray and Local Aensthetics-soaked Nasal Packings on Postoperative Pain After Nasal Closed Reduction

The Catholic University of Korea1 site in 1 country33 target enrollmentStarted: December 3, 2018Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
33
Locations
1
Primary Endpoint
postoperative pain in recovery room

Study Overview

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).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts 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)

Arms & Interventions

local anesthetic group

Experimental

local aensthetic group receive preopetaive lidocaine spray and lidocaine-bupivacine mixture-soaked nasal pacing after nasal reduction surgery

Intervention: Lidocaine (Drug)

control group

Placebo Comparator

control group receive preoperative normal saline spray and normal saline-soaked nasal packing after nasal reduction surgery

Intervention: Lidocaine (Drug)

Outcomes

Primary Outcomes

postoperative pain in recovery room

Time Frame: immediately after surgery

Using VAS, postoperative pain is measured.

Secondary Outcomes

  • rescue analgesics in recovery room(1 hr after surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Young Eun Moon

Associate professor

The Catholic University of Korea

Study Sites (1)

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