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Prospective Evaluation of Topical Analgesia for Laceration Repair in the Emergency Department

NCT03071601 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 132

Last updated 2022-03-10

No results posted yet for this study

Summary

The purpose of this study is to determine if topical analgesia using a lidocaine and prilocaine cream improves pain scores compared to the usual local anesthesia using subcutaneous 1% lidocaine and adrenalin injected near the laceration.

Conditions

  • Pain, Acute
  • Laceration

Interventions

DRUG

Lidocaine-Prilocaine Cream 2.5-2.5%

Topical anesthesia using a cream containing 2.5% Lidocaine and 2.5 % Prilocaine for at least 30 minutes on and around the wound before suture

DRUG

Lidocaine 1% Epinephrine 0.005mg/mL solution

Local anesthesia by subcutaneous injection of a solution containing 1% Lidocaine and 0.005mg/mL Epinephrine in and around the wound in the minutes preceding the suture of the wound

Sponsors & Collaborators

  • University Hospital, Angers

    collaborator OTHER_GOV

  • Centre Hospitalier le Mans

    lead OTHER

Principal Investigators

  • Julien Fonsegrive, MD · Centre Hospitalier le Mans

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-12-01
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03071601 on ClinicalTrials.gov