Determination of Nerve Growth Factor (NGF) Expression in Pediatric Patients With Severe Burns: a Pilot Study

Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS (Other)
Overall Status
Completed
CT.gov ID
NCT05751174
Collaborator
(none)
12
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Study Details

Study Description

Brief Summary

The goal of this observational study is to determine the blood values of NGF in severely burned patients, to describe any changes over time and finally to correlate the expression of NGF to the severity of the burn.

The main question it aims to answer is:
  • describe NGF values in severely burned pediatric patients and to evaluate their correlation with the severity of the burn and the extent of the burned skin surface by measuring the circulating levels of NGF in pediatric patients.

Participants will undergo blood sampling on days 2,7,14 and 30 after the traumatic event for the clinical follow-up envisaged by the internal protocol.

Condition or Disease Intervention/Treatment Phase
  • Other: pediatric patients affected by severe burns

Detailed Description

Severe pediatric burns, characterized by an extension greater than 10% of the total body surface or by the involvement of particular districts such as the hands, face, airways or genitals, are characterized by multisystem involvement, which often requires intensive care support.

The epidermis begins to develop from the superficial ectoderm at the end of the fourth week of gestation when the neural tube separates from the overlying ectoderm. Consequently, the ectoderm gives rise to both the nervous system and the epithelium.

In particular, the NERVE GROWTH FACTOR (NGF) is a neurotrophic factor that plays a fundamental protective role in the development and survival of neurons.

In fetal skin, NGF is synthesized in both the epithelium and mesenchyme, but the highest amounts of NGF messenger ribonucleic acid are found in the epithelium. There are currently no studies investigating the expression of NGF in severe burns.

The common embryonic origin of the skin and the neurological system may hold the key to new research opportunities to understand the regenerative response and in particular the role of growth factors such as NGF in the skin repair mechanism in severe burns .

The hypothesis of the study is based on the possibility that skin burns may be related to an increased expression of circulating NGF in the blood. However, there are no data in literature on this issue and the behavior of NGF in patients affected by burns is not known, either in adult or pediatric patients.

Aim To describe NGF values in severely burned pediatric patients and to evaluate their correlation with the severity of the burn and the extent of the burned skin surface by measuring the circulating levels of NGF.

Study Design

Study Type:
Observational
Actual Enrollment :
12 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Determination of Nerve Growth Factor (NGF) Expression in Pediatric Patients With Severe Burns: a Pilot Study
Actual Study Start Date :
Mar 18, 2021
Actual Primary Completion Date :
May 26, 2022
Actual Study Completion Date :
Aug 30, 2022

Outcome Measures

Primary Outcome Measures

  1. Qualitative description of NGF values in severely burned pediatric patients. [up to 30 days]

    Patients will undergo blood sampling on days 2,7,14 and 30 after the traumatic event for the clinical follow-up envisaged by the internal protocol. A small aliquot of blood (5 ml) will be dedicated separately for the measurement of circulating NGF levels

Secondary Outcome Measures

  1. To evaluate the correlation of the extent of NGF expression with the severity of the burn and with the extent of the burned skin surface. [From date of inclusion in the study until 30 days after admission in pediatric intensive care]

    In the protocol we will collect the following demographic and clinical variables: Age, gender, weight, total body surface area (%), Burn depth I II III degree, specific surface involvement (face, genitals, palms and soles), organ failure, use of inotropic and vasoconstrictor drugs, need for intubation and mechanical ventilation, quantification of fluid therapy for shock correction, infectious complications, need for surgery with possible homologous/autologous skin graft. these variables will be included to assess the correlation with NGF values

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients suffering from severe burns
Exclusion Criteria:
  • Major congenital malformations

  • Antibiotic treatment 48 hours prior to admission

  • Norepinephrine infusion > 0.5 mcg/k/min

  • Lack of informed consent from parents or legal guardians

Contacts and Locations

Locations

Site City State Country Postal Code
1 Giorgio Conti Rome Italy 00168

Sponsors and Collaborators

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Investigators

  • Principal Investigator: Giorgio GC Conti, Professor, Fondazione Policlinico Gemelli IRCCS, Rome

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Conti Giorgio, Professor, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
ClinicalTrials.gov Identifier:
NCT05751174
Other Study ID Numbers:
  • 3935
First Posted:
Mar 2, 2023
Last Update Posted:
Mar 2, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Conti Giorgio, Professor, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 2, 2023