NCT07350811

Brief Summary

The main part of the study is a retrospective analysis of 200 reports concerning patients with skin wounds and injuries :

  • 50 consecutive patient reports dealing with skin lacerations
  • 50 consecutive patient reports dealing with skin abrasions
  • 50 consecutive patient reports dealing with skin burns
  • 50 consecutive patient reports dealing with leg ulcers The study comprises a complementary prospective segment, consisting of data collection from patients and from care delivery personnel, threw short interviews, in order to assess the validity of the retrospective recording on reports.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
240

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 11, 2024

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

November 6, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2025

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2025

Completed
6 months until next milestone

First Posted

Study publicly available on registry

January 20, 2026

Completed
Last Updated

January 20, 2026

Status Verified

January 1, 2026

Enrollment Period

7 months

First QC Date

November 6, 2024

Last Update Submit

January 9, 2026

Conditions

Keywords

Procedural analgesiaSkin injuries

Outcome Measures

Primary Outcomes (1)

  • Pain level

    Pain level ≤ 3/10 (light or no pain) on a 10-point pain scale throughout the interval starting 30 minutes after treatment initiation and ending.

    Up to 30 minutes

Study Arms (4)

Procedural analgesia delivered to patients with dermabrasion

Hospital reports of patients who were treated in the emergency deparment for skin abrasion

Procedural analgesia delivered to patients with skin burn

Hospital reports of patients who were treated in the emergency department for skin burn

Procedural analgesia delivered to patients with leg ulcer

Hospital reports of patients who were treated in the vascular department for leg ulcer

Procedural analgesia delivered to patients with skin lacerations

Hospital reports of patients who were treated in the emergency deparment for skin lacerations

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult patients with skin injuries (consulting emergency departments for skin laceration abrasion or burn, consulting vascular unit for patients with leg ulcer).

You may qualify if:

  • Main retrospective study: Adult patient with skin injury (laceration, abrasion, burn or skin ulcer) whose medical report is available.
  • Additionnal prospective interview: Adult patient with skin injury (laceration, abrasion, burn or skin ulcer) who consents to the 10-minute interview.

You may not qualify if:

  • Main retrospective study: medical report incomplete. Additionnal prospective interview: Not french speaking.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hospital Versailles

Le Chesnay, 78150, France

Location

MeSH Terms

Conditions

ParesthesiaLeg Ulcer

Condition Hierarchy (Ancestors)

Somatosensory DisordersSensation DisordersNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsSkin UlcerSkin DiseasesSkin and Connective Tissue Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Investigator Coordonnator

Study Record Dates

First Submitted

November 6, 2024

First Posted

January 20, 2026

Study Start

June 11, 2024

Primary Completion

January 15, 2025

Study Completion

July 15, 2025

Last Updated

January 20, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Clinical, treatment and logistical data will be anonymously be recorded (ther will be no mention of age, gender, name, letters or numbers to identify participants): IPD will not be collected and therefore not shared.

Locations