NCT04124133

Brief Summary

Observational retrospective monocentric study occured in the univeristy hospital center of Bensançon the department of pediatric surgery. Data of patients treated in the hospital between January 2016 and January 2019 have been collected.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
92

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2018

Shorter than P25 for all trials

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

December 10, 2018

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 18, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 18, 2019

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

October 10, 2019

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 11, 2019

Completed
Last Updated

October 11, 2019

Status Verified

October 1, 2019

Enrollment Period

4 months

First QC Date

October 10, 2019

Last Update Submit

October 10, 2019

Conditions

Outcome Measures

Primary Outcomes (1)

  • Patient rate with complete healing

    pourcentage of patient with 100% of reepithelilisation

    21 days

Interventions

Application of ialuset cream or gauzepad (hyaluronic acid)

Eligibility Criteria

Age1 Month - 15 Years
Sexall
Age GroupsChild (0-17)
Sampling MethodProbability Sample
Study Population

Children from 1month to 15 years with a second degree burn

You may qualify if:

  • second-degree burns
  • less than 20% of the body surface
  • less than 15 years old
  • treated within 24 hours
  • st line of treatment with ialuset
  • treated at the center between 2016 and 2019

You may not qualify if:

  • patient who refused data collection

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Besançon

Besançon, France

Location

MeSH Terms

Interventions

Bandages

Intervention Hierarchy (Ancestors)

Equipment and Supplies

Study Officials

  • Arnaud Fotso Kamdem

    CHU Besançon

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 10, 2019

First Posted

October 11, 2019

Study Start

December 10, 2018

Primary Completion

April 18, 2019

Study Completion

April 18, 2019

Last Updated

October 11, 2019

Record last verified: 2019-10

Data Sharing

IPD Sharing
Will not share

Locations