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Casting Versus Flexible Intramedullary Nailing in Displaced Pediatric Forearm Shaft Fractures

Primary Purpose

Both Bone Forearm Fracture, AO Classification 22D/2.1-5.2, 7-12 Year Old

Status
Recruiting
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
Flexible intramedullary nail (FIN)
Reduction auder general anesthesia and long arm cast
Sponsored by
Helsinki University Central Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Both Bone Forearm Fracture

Eligibility Criteria

7 Years - 12 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 7 to12 year old children
  • Open distal radial physis
  • Both bone forearm shaft fractures (AO-pediatric classification: 22D/2.1-5.2)
  • More than 10 degrees of angulation
  • with or without less than 10mm of shortening

Exclusion Criteria:

  • Patients with bilateral fractures
  • Gustilo-Anderson grade I-III open fracture
  • Neurovascular deficit
  • Compartment syndrome
  • Pathologic fracture
  • Patient not able to give a written informed consent

Sites / Locations

  • HUS New Childrens HospitalRecruiting
  • Kuopio University HospitalRecruiting
  • Oulu University Hospital
  • Tampere University Hospital
  • Turku University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Other

Other

Arm Label

FIN (Flexible intramedullary nail)

Long arm cast

Patient Choice FIN

Patient Choice cast

Arm Description

Fracture reduction and fixation using flexible intramedullary nails. Nails size is 0.4 times the smallest diameter of the medullary canal of radius or ulna measured in radiographs.

Fractures are reduced under general anesthesia within 3 days from injury and a synthetic circular above elbow cast in neutral pro-supination is applied for six weeks.

Fracture reduction and fixation using flexible intramedullary nails. Nails size is 0.4 times the smallest diameter of the medullary canal of radius or ulna measured in radiographs.

Fractures are reduced under general anesthesia within 3 days from injury and a synthetic circular above elbow cast in neutral pro-supination is applied for six weeks.

Outcomes

Primary Outcome Measures

PROMIS Pediatric Item Bank v2.0 - Upper Extremity
We aim to confirm that 75 percent of FIN patients have a better PROMIS UE score than what the mean score of the cast patients will be assuming both groups have the same standard deviation. PROMIS (Patient-Reported Outcomes Measurement Information System) scores are normalized to a mean score of 50, standard deviation of 10, with a theoretical range of 0 to 100. A higher score corresponds to a greater amount of the domain being measured.
Pro-supination
Difference (percent) in forearm pronation-supination range of motion (ROM) at one-year follow-up in comparison to uninjured side.

Secondary Outcome Measures

Quick Disabilities of the Arm, Shoulder and Hand score
Minimum value is 0 and maximum 100. Higher value indicates worse function. Statistically significant difference in QuickDASH score is 6.8 (18) at 12 months FU.
Measurement Model for the Pediatric Quality of Life Inventory (PedsQL)
Minimum value is 0 and maximum value is 100. Higher score indicates better health related quality of life.
Measurement Model for the Pediatric Quality of Life Inventory Pediatric Pain Questionaire (PEDS QL PPQ)
Minimum value 0 maximum value 10. Higher value indicates higher pain intensity
Need for re-interventions
Minimum value 0 no maximum value. Lower value indicates better outcome.
Rate of participants with malunion
malunion, delayed union (defined as nonunion at 3 months or later), pseudoarthrosis (defined as 3 cortices out of 4 not united at 6 months or later)
Adverse effects
adverse effects (wound infection, nerve or/and tendon damage)
Cosmetic VAS
Minimum value 0 maximum value 10. Higher value indicates better satisfaction
PROMIS Pediatric Item Bank v2.0 - Upper Extremity
Difference between treatment groups
Upper limb ROM
Difference (percent) in elbow, wrist flexion extension and pronation-supination in comparison to uninjured side
Return to sport/musical instrument and level
Level of practiced sport or musical instrument before and at end of trial, as well as time from injury to return to hobby is registered.

Full Information

First Posted
December 6, 2020
Last Updated
July 23, 2021
Sponsor
Helsinki University Central Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04664517
Brief Title
Casting Versus Flexible Intramedullary Nailing in Displaced Pediatric Forearm Shaft Fractures
Official Title
Casting Versus Flexible Intramedullary Nailing in Displaced Forearm Shaft Fractures in 7 to 12 Years Old Children: A Study Protocol for a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2021 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Helsinki University Central Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The forearm is the most common fracture location in children, with an increasing incidence. Displaced forearm shaft fractures have traditionally been treated with closed reduction and cast immobilization. Diaphyseal fractures in children have poor remodeling capacity, and malunion can thus cause permanent cosmetic and functional disability. Internal fixation especially with flexible intramedullary nails has gained increasing popularity, without evidence of a better outcome compared to closed reduction and cast immobilization.
Detailed Description
This is a multicenter, randomized superiority trial comparing closed reduction and cast immobilization to flexible intramedullary nails in 7-12 year old children with > 10° of angulation and/or > 10mm of shortening in displaced both bone forearm shaft fractures (AO-pediatric classification: 22D/2.1-5.2). A total of 78 patients with minimum 2 years of expected growth left are randomized in 1:1 ratio to either treatment group. The study has a parallel non-randomized patient preference arm. Both treatments are performed under general anesthesia. In the cast group a long arm cast is applied for 6 weeks. The flexible intramedullary nail group is immobilized in a collar and cuff sling for 4 weeks. Data is collected at baseline and at each follow-up until 1 year. Primary outcome is 1) PROMIS Pediatric Item Bank v2.0 - Upper Extremity and 2) forearm pronation-supination range of motion at one-year follow-up. Secondary outcomes are Quick DASH, Pediatric pain questionnaire, Cosmetic VAS, wrist range of motion as well as any complications (malunion, delayed union, non-union or deep wound infection, peripheral nerve injury, need for re-intervention during 1-year follow-up) and costs of treatment. The investigators hypothesize that flexible intramedullary nailing results in a superior outcome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Both Bone Forearm Fracture, AO Classification 22D/2.1-5.2, 7-12 Year Old

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
multicenter, randomized superiority trial. Parallell patient choice arm.
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
FIN (Flexible intramedullary nail)
Arm Type
Active Comparator
Arm Description
Fracture reduction and fixation using flexible intramedullary nails. Nails size is 0.4 times the smallest diameter of the medullary canal of radius or ulna measured in radiographs.
Arm Title
Long arm cast
Arm Type
Active Comparator
Arm Description
Fractures are reduced under general anesthesia within 3 days from injury and a synthetic circular above elbow cast in neutral pro-supination is applied for six weeks.
Arm Title
Patient Choice FIN
Arm Type
Other
Arm Description
Fracture reduction and fixation using flexible intramedullary nails. Nails size is 0.4 times the smallest diameter of the medullary canal of radius or ulna measured in radiographs.
Arm Title
Patient Choice cast
Arm Type
Other
Arm Description
Fractures are reduced under general anesthesia within 3 days from injury and a synthetic circular above elbow cast in neutral pro-supination is applied for six weeks.
Intervention Type
Procedure
Intervention Name(s)
Flexible intramedullary nail (FIN)
Intervention Description
Both bone FIN
Intervention Type
Procedure
Intervention Name(s)
Reduction auder general anesthesia and long arm cast
Intervention Description
Reduction and cast
Primary Outcome Measure Information:
Title
PROMIS Pediatric Item Bank v2.0 - Upper Extremity
Description
We aim to confirm that 75 percent of FIN patients have a better PROMIS UE score than what the mean score of the cast patients will be assuming both groups have the same standard deviation. PROMIS (Patient-Reported Outcomes Measurement Information System) scores are normalized to a mean score of 50, standard deviation of 10, with a theoretical range of 0 to 100. A higher score corresponds to a greater amount of the domain being measured.
Time Frame
12 months
Title
Pro-supination
Description
Difference (percent) in forearm pronation-supination range of motion (ROM) at one-year follow-up in comparison to uninjured side.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Quick Disabilities of the Arm, Shoulder and Hand score
Description
Minimum value is 0 and maximum 100. Higher value indicates worse function. Statistically significant difference in QuickDASH score is 6.8 (18) at 12 months FU.
Time Frame
6 weeks, 3, 6 and 12 months
Title
Measurement Model for the Pediatric Quality of Life Inventory (PedsQL)
Description
Minimum value is 0 and maximum value is 100. Higher score indicates better health related quality of life.
Time Frame
6 weeks, 3, 6 and 12 months
Title
Measurement Model for the Pediatric Quality of Life Inventory Pediatric Pain Questionaire (PEDS QL PPQ)
Description
Minimum value 0 maximum value 10. Higher value indicates higher pain intensity
Time Frame
6 weeks, 3, 6 and 12 months
Title
Need for re-interventions
Description
Minimum value 0 no maximum value. Lower value indicates better outcome.
Time Frame
6 weeks, 3, 6 and 12 months
Title
Rate of participants with malunion
Description
malunion, delayed union (defined as nonunion at 3 months or later), pseudoarthrosis (defined as 3 cortices out of 4 not united at 6 months or later)
Time Frame
6 weeks, 3, 6 and 12 months
Title
Adverse effects
Description
adverse effects (wound infection, nerve or/and tendon damage)
Time Frame
6 weeks, 3, 6 and 12 months
Title
Cosmetic VAS
Description
Minimum value 0 maximum value 10. Higher value indicates better satisfaction
Time Frame
6 weeks, 3, 6 and 12 months
Title
PROMIS Pediatric Item Bank v2.0 - Upper Extremity
Description
Difference between treatment groups
Time Frame
6 weeks, 3, 6 months
Title
Upper limb ROM
Description
Difference (percent) in elbow, wrist flexion extension and pronation-supination in comparison to uninjured side
Time Frame
6 weeks, 3, 6 months
Title
Return to sport/musical instrument and level
Description
Level of practiced sport or musical instrument before and at end of trial, as well as time from injury to return to hobby is registered.
Time Frame
6 weeks, 3, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 7 to12 year old children Open distal radial physis Both bone forearm shaft fractures (AO-pediatric classification: 22D/2.1-5.2) More than 10 degrees of angulation with or without less than 10mm of shortening Exclusion Criteria: Patients with bilateral fractures Gustilo-Anderson grade I-III open fracture Neurovascular deficit Compartment syndrome Pathologic fracture Patient not able to give a written informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Petra Grahn, MD
Phone
+35894711
Email
petra.grahn@hus.fi
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ilkka Helenius, MD
Organizational Affiliation
Helsinki University Central Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Petra Grahn, MD
Organizational Affiliation
Helsinki University Central Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
HUS New Childrens Hospital
City
Helsinki
ZIP/Postal Code
00029HUS
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Petra Grahn, MD
Phone
+358 9 4711
First Name & Middle Initial & Last Name & Degree
Matti Ahonen, MD
Phone
+ 358 9 4711
Facility Name
Kuopio University Hospital
City
Kuopio
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yrjänä Nietosvaara, MD
Facility Name
Oulu University Hospital
City
Oulu
Country
Finland
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juha-Jaakko Sinikumpu, MD
Facility Name
Tampere University Hospital
City
Tampere
Country
Finland
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne Salonen, MD
Facility Name
Turku University Hospital
City
Turku
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Johanna Syvänen, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All data will be available upon request. Data will be delivered as anonymized.
IPD Sharing Time Frame
Study protocol is published in BMJ open. What can not be found there can be shared by contacting the main investigator.
IPD Sharing Access Criteria
Please see the study protocol in BMJ open
Citations:
PubMed Identifier
34417215
Citation
Grahn P, Sinikumpu JJ, Nietosvaara Y, Syvanen J, Salonen A, Ahonen M, Helenius I. Casting versus flexible intramedullary nailing in displaced forearm shaft fractures in children aged 7-12 years: a study protocol for a randomised controlled trial. BMJ Open. 2021 Aug 20;11(8):e048248. doi: 10.1136/bmjopen-2020-048248.
Results Reference
derived
Links:
URL
https://bmjopen.bmj.com/
Description
Protocol publication

Learn more about this trial

Casting Versus Flexible Intramedullary Nailing in Displaced Pediatric Forearm Shaft Fractures

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