Comparison of 2 Application Techniques for LET Gel Used Prior to Simple Laceration Repair (LET)
Primary Purpose
LET, Laceration of Skin
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
LET (lidocaine 4%; epinephrine 0.1%; tetracaine 0.5%) gel (1 application)
LET (lidocaine 4%; epinephrine 0.1%; tetracaine 0.5%) gel (3 applications)
Sponsored by
About this trial
This is an interventional treatment trial for LET
Eligibility Criteria
Inclusion Criteria:
- • Patients with simple (< 3 cm) lacerations who are > 7 years old and < 18 years old, for whom the physician plans to close the laceration using simple superficial interrupted sutures.
Exclusion Criteria:
• Lacerations involving the hands, feet, genitals, tongue, mucus membranes, nose, ears, or occurring over joints.
- Patients who are developmentally delayed or have a disability preventing them from giving a reliable pain score.
- Patients whose primary language is other than English or Spanish.
- Patients for whom procedural sedation is required.
- Patients receiving intranasal or oral midazolam or inhaled nitrous oxide.
Sites / Locations
- CHOC Children's
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1 application
3 applications
Arm Description
Patients receive single dose LET
Patients receive 3 doses of LET
Outcomes
Primary Outcome Measures
To compare pain scores
Visual Analog Scale (VAS) asks subjects to rate pain marking an X on a line between two ends: "No pain" (on the left) and "Pain as bad as it could possibly be" (on the right). The distance will be measured from "No pain" to the X placed by the subject. A higher measurement indicates more pain.
Secondary Outcome Measures
To compare provider satisfaction scores
Likert scale will be used in 3 questions asking providers to rate their satisfaction, preference for Single LET application, and preference for Triple LET application. For the satisfaction question, the likert scale offers options from Dissatisfied to Extremely Satisfied, as well as Not Applicable. The preference for Single LET is a likert scale with options ranging from Strongly Disagree to Strongly Agree, as well as a Not Applicable. The preference for Triple LET is a likert scale with options ranging from Strongly Disagree to Strongly Agree, as well as a Not Applicable. It will take approximately 3 minutes to administer. This measure will be completed once for each enrollment prior to discharge from the Emergency Department.
To compare parental satisfaction scores
Parent satisfaction will be measured using a single question as a Likert scale with options from Dissatisfied to Extremely Satisfied, as well as Not Applicable. It will take approximately 1-2 minutes to administer. This measure will be completed once for each enrollment prior to discharge from the Emergency Department.
Full Information
NCT ID
NCT04536493
First Posted
June 20, 2019
Last Updated
September 1, 2020
Sponsor
Children's Hospital of Orange County
1. Study Identification
Unique Protocol Identification Number
NCT04536493
Brief Title
Comparison of 2 Application Techniques for LET Gel Used Prior to Simple Laceration Repair
Acronym
LET
Official Title
Comparison of 2 Application Techniques for LET (Lidocaine 4%; Epinephrine 0.1%; Tetracaine 0.5%) Gel Used Prior to Simple Laceration Repair
Study Type
Interventional
2. Study Status
Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
June 19, 2019 (Actual)
Primary Completion Date
November 6, 2019 (Actual)
Study Completion Date
June 25, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Hospital of Orange County
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
To compare pain scores during laceration repair with first suture placement using standardized visual analog scale (VAS) between 2 different topical local anesthetic application techniques for using LET gel. Specifically, the investigators are studying if applying LET gel 3 times, spaced 10 minutes apart (triple LET) provides superior anesthesia to one 30 minute application (single LET). Single LET is the current standard method of application.
Detailed Description
To compare pain scores during laceration repair with first suture placement using standardized visual analog scale (VAS) between 2 different topical local anesthetic application techniques for using LET gel. Specifically, the investigators are studying if applying LET gel 3 times, spaced 10 minutes apart (triple LET) provides superior anesthesia to one 30 minute application (single LET).
Secondary endpoints:
To compare provider satisfaction scores using a Likert scale between the triple LET and single LET application techniques.
To compare parental satisfaction scores using a Likert scale between the triple LET and single LET application techniques.
To compare the need for additional local anesthetic infiltration between the triple LET and single LET application techniques.
Once patients are identified and consent is obtained, they will be randomized to one of two groups. One group will have LET gel applied to the laceration one time for a duration of 30 minutes. The other group will have LET gel applied 3 times, at 10 minute intervals. Between applications, the excess gel on the surface of the skin will be gently wiped off, and a new strip of LET gel will be applied. The laceration repair will proceed in a normal sterile fashion, using standard irrigation and debridement techniques. Laceration repair will occur within the 15 minutes following the 30 minute period of LET application to the wound. The patient will be asked to rate his/her pain immediately after the first suture is placed or attempted using the visual analogue scale (VAS, range 0-10). The decision to use any additional anesthetic infiltration will be left to the performing provider. There will be 2 nurses involved in the study. One nurse will be the patient's primary nurse and will be administering the LET gel (so will not be blinded, but will not be involved in data collection). The other nurse will be obtaining the VAS immediately (Appendix 3) after the first suture is placed, using a pre-prepared script (Appendix 3) and standardized technique. The nurse or research assistant will also be blinded as to the method of LET gel application. The provider performing the laceration repair will be blinded. The research assistant will not be blinded and will coordinate all involved providers and nurses, will ensure correct timing in LET gel administration, and laceration repair timing.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
LET, Laceration of Skin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial comparing two different applications of LET gel in pediatric patients with minor lacerations.
Masking
Care ProviderInvestigatorOutcomes Assessor
Masking Description
Topical anesthetic applied by RN not involved in procedure.
Allocation
Randomized
Enrollment
48 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1 application
Arm Type
Active Comparator
Arm Description
Patients receive single dose LET
Arm Title
3 applications
Arm Type
Active Comparator
Arm Description
Patients receive 3 doses of LET
Intervention Type
Drug
Intervention Name(s)
LET (lidocaine 4%; epinephrine 0.1%; tetracaine 0.5%) gel (1 application)
Other Intervention Name(s)
LET gel
Intervention Description
1 application of LET topical anesthetic gel
Intervention Type
Drug
Intervention Name(s)
LET (lidocaine 4%; epinephrine 0.1%; tetracaine 0.5%) gel (3 applications)
Other Intervention Name(s)
LET gel
Intervention Description
3 applications of LET topical anesthetic gel
Primary Outcome Measure Information:
Title
To compare pain scores
Description
Visual Analog Scale (VAS) asks subjects to rate pain marking an X on a line between two ends: "No pain" (on the left) and "Pain as bad as it could possibly be" (on the right). The distance will be measured from "No pain" to the X placed by the subject. A higher measurement indicates more pain.
Time Frame
The VAS to rate pain will be collected during laceration repair, immediately after the first suture placement or attempt. The VAS score is estimated to take up to 1 minute to collect. The VAS scale will be collected for each enrolled subject.
Secondary Outcome Measure Information:
Title
To compare provider satisfaction scores
Description
Likert scale will be used in 3 questions asking providers to rate their satisfaction, preference for Single LET application, and preference for Triple LET application. For the satisfaction question, the likert scale offers options from Dissatisfied to Extremely Satisfied, as well as Not Applicable. The preference for Single LET is a likert scale with options ranging from Strongly Disagree to Strongly Agree, as well as a Not Applicable. The preference for Triple LET is a likert scale with options ranging from Strongly Disagree to Strongly Agree, as well as a Not Applicable. It will take approximately 3 minutes to administer. This measure will be completed once for each enrollment prior to discharge from the Emergency Department.
Time Frame
The provider satisfaction Likert scale will be collected immediately after the procedure.
Title
To compare parental satisfaction scores
Description
Parent satisfaction will be measured using a single question as a Likert scale with options from Dissatisfied to Extremely Satisfied, as well as Not Applicable. It will take approximately 1-2 minutes to administer. This measure will be completed once for each enrollment prior to discharge from the Emergency Department.
Time Frame
The parental satisfaction Likert scale will be collected immediately after the procedure.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
• Patients with simple (< 3 cm) lacerations who are > 7 years old and < 18 years old, for whom the physician plans to close the laceration using simple superficial interrupted sutures.
Exclusion Criteria:
• Lacerations involving the hands, feet, genitals, tongue, mucus membranes, nose, ears, or occurring over joints.
Patients who are developmentally delayed or have a disability preventing them from giving a reliable pain score.
Patients whose primary language is other than English or Spanish.
Patients for whom procedural sedation is required.
Patients receiving intranasal or oral midazolam or inhaled nitrous oxide.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joshua Siembieda
Organizational Affiliation
CHOC Childrens
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHOC Children's
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
23897942
Citation
Harman S, Zemek R, Duncan MJ, Ying Y, Petrcich W. Efficacy of pain control with topical lidocaine-epinephrine-tetracaine during laceration repair with tissue adhesive in children: a randomized controlled trial. CMAJ. 2013 Sep 17;185(13):E629-34. doi: 10.1503/cmaj.130269. Epub 2013 Jul 29.
Results Reference
background
PubMed Identifier
12827121
Citation
Priestley S, Kelly AM, Chow L, Powell C, Williams A. Application of topical local anesthetic at triage reduces treatment time for children with lacerations: a randomized controlled trial. Ann Emerg Med. 2003 Jul;42(1):34-40. doi: 10.1067/mem.2003.207.
Results Reference
background
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Comparison of 2 Application Techniques for LET Gel Used Prior to Simple Laceration Repair
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