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Evaluation of Functional Outcomes at 2 Months According to Therapeutic Management, in Trauma With Low-grade Osteo-ligamentous Ankle Injury in Children (CHEVIPED)

Primary Purpose

Ankle Injuries, Ligament Injury

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
below-knee soft resin cast
Below-knee rigid resin cast
Sponsored by
University Hospital, Brest
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ankle Injuries focused on measuring low-grade, osteo-ligament injuries, children, soft resin ankle brace, Below-knee rigid resin cast

Eligibility Criteria

5 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Walking child from 5 to 15 years old.
  • From hour 0 to hour 48 of ankle trauma with torsion mechanism (inversion, eversion or rotation).
  • Patient presenting for the first time to the emergency room for this traumatic episode.
  • Possibility of carrying out an ultrasound during the passage to the emergency room.
  • Child and parents' consent in the study participation

Exclusion Criteria:

  • Direct shock on the foot without sprain mechanism.
  • Fracture with deformation or open fracture.
  • History of ankle trauma in the last 3 months.
  • Neurological or neuromuscular pathology.
  • Child with a delay in acquisitions and / or psychomotor development (difficulties in understanding and interacting to locate pain).
  • Absence of a representative of parental authority.
  • Constitutional bone disease or connective tissue.
  • Acquired or congenital coagulopathy.
  • Patient presenting beyond 48h of trauma.
  • Polytraumatized.
  • Dermabrasion, wound or sign of skin suffering next to the ankle requiring specific monitoring.
  • Diagnosis after imaging: fracture or sprain of high grade.
  • Child or parents refusal in study participation

Sites / Locations

  • CHU de BrestRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Below-knee soft resin cast

Below-knee rigid resin cast

Arm Description

Below-knee soft resin cast is administered to participants in emergency department. Investigator puts three layers of jersey supplemented by strips of soft resins to be unrolled along the leg after immersion in warm water Duration to ankle immobilization with soft resin boot : 21 days.

Below-knee soft resin cast is administered to participants in emergency department. Investigator puts one layer of jersey and then one layer of foam composed by strips of cotton wool to be unrolled supplemented by strips of rigid resins to be unrolled along the leg after immersion in warm water. Duration to ankle immobilization with soft resin boot : 21 days.

Outcomes

Primary Outcome Measures

Activities Scale for Kids (ASKp)
Activities Scale for Kids (ASKp) is a questionnaire about activities from the previous week. It has 30 item with 5 answers : all of the time (the better) / most of the time / sometimes / once in a while / none of the time (the worse).

Secondary Outcome Measures

Visual Analogue Scale (VAS)
It is a scale that measures pain intensity with small ruler, between 0 (no pain) to 10 (severe pain). It can be administered for children 4 to 6 years old.
Visual Analogue Scale (VAS)
It is a scale that measures pain intensity with small ruler, between 0 (no pain) to 10 (severe pain). It can be administered for children 4 to 6 years old.
Numeric Scale (NS)
It is a scale that mesures pain intensity. Children aged to 4 to 6 years gives a grade between 0 (no pain) to 10 (severe pain)
Numeric Scale (NS)
It is a scale that measures pain intensity. Children aged to 4 to 6 years gives a grade between 0 (no pain) to 10 (severe pain)
Clinical exams
Clinical exams are exams administered by investigator during a consultation. There are four exams : inspection : presence or not of a hematoma and oedema palpation : pain or not with palpation mobilization : 3 items with 2 answers (Yes/No) support capacity : 2 items with 2 answers (Yes/No)
Clinical exams
Clinical exams are exams administered by investigator during a consultation. There are four exams : inspection : presence or not of a hematoma and oedema palpation : pain or not with palpation mobilization : 3 items with 2 answers (Yes/No) support capacity : 2 items with 2 answers (Yes/No)
Parents questionnaire
It is a questionnaire for parents that assesses the feeling about the children care, with 3 questions.
Intercurrent consultation
Adjudicated intercurrent consultation (Other medical consultation than those planned) during the study treatment period
injury during removal of the device
Adjudicated injury during removal of the device during the study treatment period
Negative predictive value (VPN) of "combined clinical criteria"
Negative predictive value (VPN) of "combined clinical criteria" in the detection of low-grade bone or ligament damage to the ankle in children compared to ultrasound/radiography.
Sensitivity and specificity of local skin signs
Sensitivity and specificity of local skin signs (INSPECTION line of the clinical examination questionnaire) to detect high-grade ligament damage on ultrasound.
Comparison between clinical exams and the radiography results.
Clinical exams are exams administred by investigator during a consultation (inspection, palpation, mobilization, support capacity).The results of this exams are compared to radiography results at the inclusion (origin and localization of injury)
Comparison between the clinical exams and the ultrasound results.
Clinical exams are exams administred by investigator during a consultation (inspection, palpation, mobilization, support capacity).The results of this exams are compared to ultrasound results at the inclusion (origin and localization of injury) .
Comparison between the radiography results and the ultrasound results.
Ultrasound results are compared to radiography results at the inclusion (origin and localization of injury) .

Full Information

First Posted
August 6, 2021
Last Updated
July 11, 2023
Sponsor
University Hospital, Brest
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1. Study Identification

Unique Protocol Identification Number
NCT05009342
Brief Title
Evaluation of Functional Outcomes at 2 Months According to Therapeutic Management, in Trauma With Low-grade Osteo-ligamentous Ankle Injury in Children
Acronym
CHEVIPED
Official Title
Evaluation of Functional Outcomes at 2 Months According to Therapeutic Management, in Trauma With Low-grade Osteo-ligamentous Ankle Injury in Children
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 9, 2021 (Actual)
Primary Completion Date
November 9, 2024 (Anticipated)
Study Completion Date
November 9, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Brest

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Lack of current consensus on the therapeutic management of low-grade osteo-ligament injuries in ankle trauma in children. Several types of immobilization are evaluated in the literature, with different conclusions. Some teams recommend a functional treatment similar to the adult (with or without strict immobilization), others remain on standard rigid immobilizations. The goal of the study is to simplify and homogenize the therapeutic management of low-grade osteo-ligament injuries in ankle trauma in children.
Detailed Description
Lack of current consensus on the therapeutic management of low-grade osteo-ligament injuries in ankle trauma in children. Several types of immobilization are evaluated in the literature, with different conclusions. Some teams recommend a functional treatment similar to the adult (with or without strict immobilization), others remain on standard rigid immobilizations. The goal of the study is to simplify and homogenize the therapeutic management of low-grade osteo-ligament injuries in ankle trauma in children. CHEVIPED is a controlled, randomized, comparative monocentric trial. Randomization into 2 groups and stratified on presence to fracture Salter 1 and age Experimental group : Patients with below-knee soft resin cast Control group : Patients with below-knee rigid resin cast. The primary objective is to demonstrate at 2 months that with post traumatic low- grade osteo-ligamentous ankle injury the recovery of physical function are at least as effective with a below-knee soft resin cast compared to a below-knee rigid resin cast. The secondary objectives are : Clinical evaluation of treatment at 3 weeks in immediate post-immobilization. Evaluation of the management satisfaction (effectiveness and understanding) and the treatment tolerance . Evaluation of the time taken to resume painless support after immobilization. Point of interest evaluation Determine the diagnostic performance of the "combined clinical criteria" in comparison with the ultrasound/radiography couple. Evaluation of the diagnostic performance of clinical inspection criteria (edema, bruise) in high-grade ligament damage. Evaluation of the link between the "combined clinical criteria" and the results of the radiography. Evaluation of the relationship between "combined clinical criteria" and ultrasound results. Evaluation of the link between the results of radiography and ultrasound. 200 patients are expected to be included. Inclusion period : 12 months. Duration of patient's participation: 2 months Total study duration: 14 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankle Injuries, Ligament Injury
Keywords
low-grade, osteo-ligament injuries, children, soft resin ankle brace, Below-knee rigid resin cast

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Monocentric, randomized, non-inferiority, without blinding, controlled trial with 2 parallel groups
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Below-knee soft resin cast
Arm Type
Experimental
Arm Description
Below-knee soft resin cast is administered to participants in emergency department. Investigator puts three layers of jersey supplemented by strips of soft resins to be unrolled along the leg after immersion in warm water Duration to ankle immobilization with soft resin boot : 21 days.
Arm Title
Below-knee rigid resin cast
Arm Type
Other
Arm Description
Below-knee soft resin cast is administered to participants in emergency department. Investigator puts one layer of jersey and then one layer of foam composed by strips of cotton wool to be unrolled supplemented by strips of rigid resins to be unrolled along the leg after immersion in warm water. Duration to ankle immobilization with soft resin boot : 21 days.
Intervention Type
Device
Intervention Name(s)
below-knee soft resin cast
Intervention Description
Patients have soft resin boot between day 0 (inclusion visit) and day 21 (follow-up visit n°1)
Intervention Type
Device
Intervention Name(s)
Below-knee rigid resin cast
Intervention Description
Patients have rigid resin boot between day 0 (inclusion visit) and day 21 (follow-up visit n°1)
Primary Outcome Measure Information:
Title
Activities Scale for Kids (ASKp)
Description
Activities Scale for Kids (ASKp) is a questionnaire about activities from the previous week. It has 30 item with 5 answers : all of the time (the better) / most of the time / sometimes / once in a while / none of the time (the worse).
Time Frame
At 2 months
Secondary Outcome Measure Information:
Title
Visual Analogue Scale (VAS)
Description
It is a scale that measures pain intensity with small ruler, between 0 (no pain) to 10 (severe pain). It can be administered for children 4 to 6 years old.
Time Frame
day 0
Title
Visual Analogue Scale (VAS)
Description
It is a scale that measures pain intensity with small ruler, between 0 (no pain) to 10 (severe pain). It can be administered for children 4 to 6 years old.
Time Frame
day 21
Title
Numeric Scale (NS)
Description
It is a scale that mesures pain intensity. Children aged to 4 to 6 years gives a grade between 0 (no pain) to 10 (severe pain)
Time Frame
day 0
Title
Numeric Scale (NS)
Description
It is a scale that measures pain intensity. Children aged to 4 to 6 years gives a grade between 0 (no pain) to 10 (severe pain)
Time Frame
day 21
Title
Clinical exams
Description
Clinical exams are exams administered by investigator during a consultation. There are four exams : inspection : presence or not of a hematoma and oedema palpation : pain or not with palpation mobilization : 3 items with 2 answers (Yes/No) support capacity : 2 items with 2 answers (Yes/No)
Time Frame
day 0
Title
Clinical exams
Description
Clinical exams are exams administered by investigator during a consultation. There are four exams : inspection : presence or not of a hematoma and oedema palpation : pain or not with palpation mobilization : 3 items with 2 answers (Yes/No) support capacity : 2 items with 2 answers (Yes/No)
Time Frame
day 21
Title
Parents questionnaire
Description
It is a questionnaire for parents that assesses the feeling about the children care, with 3 questions.
Time Frame
day 21
Title
Intercurrent consultation
Description
Adjudicated intercurrent consultation (Other medical consultation than those planned) during the study treatment period
Time Frame
between day 0 and day 42
Title
injury during removal of the device
Description
Adjudicated injury during removal of the device during the study treatment period
Time Frame
between day 0 and day 42
Title
Negative predictive value (VPN) of "combined clinical criteria"
Description
Negative predictive value (VPN) of "combined clinical criteria" in the detection of low-grade bone or ligament damage to the ankle in children compared to ultrasound/radiography.
Time Frame
day 0
Title
Sensitivity and specificity of local skin signs
Description
Sensitivity and specificity of local skin signs (INSPECTION line of the clinical examination questionnaire) to detect high-grade ligament damage on ultrasound.
Time Frame
day 0
Title
Comparison between clinical exams and the radiography results.
Description
Clinical exams are exams administred by investigator during a consultation (inspection, palpation, mobilization, support capacity).The results of this exams are compared to radiography results at the inclusion (origin and localization of injury)
Time Frame
day 0
Title
Comparison between the clinical exams and the ultrasound results.
Description
Clinical exams are exams administred by investigator during a consultation (inspection, palpation, mobilization, support capacity).The results of this exams are compared to ultrasound results at the inclusion (origin and localization of injury) .
Time Frame
day 0
Title
Comparison between the radiography results and the ultrasound results.
Description
Ultrasound results are compared to radiography results at the inclusion (origin and localization of injury) .
Time Frame
day 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Walking child from 5 to 15 years old. From hour 0 to hour 48 of ankle trauma with torsion mechanism (inversion, eversion or rotation). Patient presenting for the first time to the emergency room for this traumatic episode. Possibility of carrying out an ultrasound during the passage to the emergency room. Child and parents' consent in the study participation Exclusion Criteria: Pubescent patients requiring anticoagulation (menarche in girls and genital pilosity in boys). Direct shock on the foot without sprain mechanism. Fracture with deformation or open fracture. History of ankle trauma in the last 3 months. Neurological or neuromuscular pathology. Child with a delay in acquisitions and / or psychomotor development (difficulties in understanding and interacting to locate pain). Absence of a representative of parental authority. Constitutional bone disease or connective tissue. Acquired or congenital coagulopathy. Patient presenting beyond 48h of trauma. Polytraumatized. Dermabrasion, wound or sign of skin suffering next to the ankle requiring specific monitoring. Child or parents refusal in study participation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthias THEPAUT, PhD
Phone
06.63.15.16.87
Email
matthias.thepaut@chu-brest.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Aude KERDONCUFF, intern
Phone
06.32.62.54.40
Email
kerdoncuffa@outlook.fr
Facility Information:
Facility Name
CHU de Brest
City
Brest
ZIP/Postal Code
29609
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aude KERDONCUFF, Intern
Phone
06.32.62.54.40
Email
kerdoncuffa@outlook.fr

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All collected data that underlie results in a publication
IPD Sharing Time Frame
Data will be available after the publication of result and ending fifteen years following the last visit of the last patient
IPD Sharing Access Criteria
Data access requests will be reviewed by the internal committee of Brest University Hospital. Requestors will be required to sign and complete a data access agreement.

Learn more about this trial

Evaluation of Functional Outcomes at 2 Months According to Therapeutic Management, in Trauma With Low-grade Osteo-ligamentous Ankle Injury in Children

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