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Immobilization Without Reduction vs. Reduction Under General Anesthesia in Metaphyseal Fractures of the Distal Radius

Primary Purpose

Radius Fracture Distal

Status
Unknown status
Phase
Not Applicable
Locations
Colombia
Study Type
Interventional
Intervention
In situ immobilization
Reduction under general anesthesia
Sponsored by
Instituto de Ortopedia Infantil Roosevelt
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Radius Fracture Distal focused on measuring radius fracture, children, conservative treatment, distal radius

Eligibility Criteria

5 Years - 10 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children from 5 years to 10 years
  • Unilateral metaphyseal distal radius fracture
  • Fracture shortening of 0 to 10mm or angulation of 10 ° to 20 ° in the oblique plane. (AO 23-M 2-3 or 23r-M 2-3)
  • Admission in the first 14 days after the fracture

Exclusion Criteria:

  • Polytrauma: Injury Severity Score (ISS)> 16
  • Associated fracture in the same limb.
  • Neuromuscular pathology (e.g., cerebral palsy, spinal muscular atrophy, Duchenne disease)
  • Open fractures.
  • History of fractures, septic arthritis, or osteomyelitis in the same limb.
  • Neurological or vascular injury in the fractured upper limb.
  • Known alteration of bone metabolism (e.g., osteogenesis imperfecta, rickets, osteopetrosis, skeletal dysplasias, lysosomal storage diseases).
  • Congenital longitudinal deficiency.

Sites / Locations

  • Instituto RooseveltRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

In situ immobilization

Reduction under general anesthesia

Arm Description

Immobilization without reducing the radius fracture and above-elbow casting.

Radius closed reduction under general anesthesia and above-elbow casting. Percutaneous fixation with K-wires, a sugar tong splint immobilization, and a nerve block if needed.

Outcomes

Primary Outcome Measures

Upper limb function
Assess upper extremity function with PROMIS Physical Function, Upper Extremity subdomain. The investigators will apply the parent-proxy version between 5 and 7 years old and the pediatric version between 8 and 10.

Secondary Outcome Measures

Wrist range of motion
Wrist passive degrees of flexion and extension measured with a goniometer aligned with the forearm axis and the second metacarpal. Pronation and supination. The investigators will ask the patient to hold a pencil vertically with the ulnar edge of the forearm on the table and the elbow flexed 90 °. The wrist is rotated medially or laterally, respectively. One arm of the goniometer is placed on the table and the other is aligned with the pencil, the degrees obtained must be subtracted from 90 °.
Ulnar variance
The investigators will consider the ulnar variance as the distance between the most distal aspect of the metaphysis of the radius and the ulna according to the Hafner distal-distal method (DIDI).
Deformity
Angulation in the oblique plane

Full Information

First Posted
June 10, 2021
Last Updated
August 9, 2021
Sponsor
Instituto de Ortopedia Infantil Roosevelt
Collaborators
Pontificia Universidad Javeriana
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1. Study Identification

Unique Protocol Identification Number
NCT05008029
Brief Title
Immobilization Without Reduction vs. Reduction Under General Anesthesia in Metaphyseal Fractures of the Distal Radius
Official Title
Cast Immobilization Without Reduction vs. Reduction Under General Anesthesia in Metaphyseal Fractures of the Distal Radius.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 15, 2021 (Actual)
Primary Completion Date
December 15, 2022 (Anticipated)
Study Completion Date
March 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto de Ortopedia Infantil Roosevelt
Collaborators
Pontificia Universidad Javeriana

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
Distal radius metaphyseal fractures are the most frequent in the pediatric population. The current treatment for angulated or shortened fractures is effective. Still, it exposes children to anesthetic risks supported by the pain generated by the reduction. Due to the excellent remodeling capacity of bone at an early age, it is questionable whether an anatomical reduction is necessary. The clinical experiment's objective is to compare the functional result of immobilization without reducing angulated or displaced metaphyseal fractures of the distal radius against fractures brought to reduction under general anesthesia. Means difference in function subdomain of the upper limb of the PROMIS® scale is the primary outcome. The secondary results are wrist mobility, radius alignment, wrist articular relationships, and surgical complications.
Detailed Description
The participant will be recruited in one center. If participants and their parents accept to participate in this study, treatments will be randomly allocated using the Big Stick Design technique with a maximum tolerated imbalance of 2. The sequence will be generated by a research assistant who is completely independent of the study, does not know the purpose of the study and the interventions. Each of the random numbers will be stored in an opaque envelope sealed externally with the order in which they should be opened. Patient registration and follow-up information will be stored in REDCap®. Clinical and radiographic outcomes will be evaluated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Radius Fracture Distal
Keywords
radius fracture, children, conservative treatment, distal radius

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The outcomes assessor will analyze the database without knowing which treatment arm each participant was allocated. He does not work in the center where the study will be carried out, nor does he contact the participants.
Allocation
Randomized
Enrollment
152 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
In situ immobilization
Arm Type
Experimental
Arm Description
Immobilization without reducing the radius fracture and above-elbow casting.
Arm Title
Reduction under general anesthesia
Arm Type
Active Comparator
Arm Description
Radius closed reduction under general anesthesia and above-elbow casting. Percutaneous fixation with K-wires, a sugar tong splint immobilization, and a nerve block if needed.
Intervention Type
Procedure
Intervention Name(s)
In situ immobilization
Intervention Description
Immobilization with an above-elbow cast. A 2, 3, or 4-year orthopedic resident or pediatric orthopedic fellow supervised by a pediatric orthopedic surgeon will perform the procedure without reduction, sedation, or anesthesia. Analgesia will be administered with paracetamol at doses of 10-15 mg/kg/dose or tramadol 0.5-1mg/kg/dose. Supposing immobilization is not satisfactory, or the patient or family member does not authorize the procedure to be carried out by staff in training. In that case, the procedure will be supported or carried out by the pediatric orthopedic surgeon.
Intervention Type
Procedure
Intervention Name(s)
Reduction under general anesthesia
Intervention Description
The participants will receive paracetamol at 10-15 mg/kg/dose or tramadol 0.5-1 mg/kg/dose for pain control until the time of surgery. Under general anesthesia, radius closed reduction, and above-elbow casting will be performed. After the reduction maneuvers, the radius reduction is satisfactory if the translation in the coronal and sagittal planes of less than 50% and angulation in the same planes is less than 10 °. If the radius does not remain reduced, it is unstable. Unstable fractures require percutaneous fixation with K-wires, a sugar tong splint immobilization, and a nerve block. The procedures will be carried out by a 2, 3, or 4-year orthopedic resident or pediatric orthopedic fellow under the supervision of a child orthopedist. Suppose reduction is not satisfactory or the patient or parent doesn´t authorize the procedure performed by personnel in training. In that case, the procedure will be supported or carried out by the pediatric orthopedic surgeon.
Primary Outcome Measure Information:
Title
Upper limb function
Description
Assess upper extremity function with PROMIS Physical Function, Upper Extremity subdomain. The investigators will apply the parent-proxy version between 5 and 7 years old and the pediatric version between 8 and 10.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Wrist range of motion
Description
Wrist passive degrees of flexion and extension measured with a goniometer aligned with the forearm axis and the second metacarpal. Pronation and supination. The investigators will ask the patient to hold a pencil vertically with the ulnar edge of the forearm on the table and the elbow flexed 90 °. The wrist is rotated medially or laterally, respectively. One arm of the goniometer is placed on the table and the other is aligned with the pencil, the degrees obtained must be subtracted from 90 °.
Time Frame
3 and 6 months
Title
Ulnar variance
Description
The investigators will consider the ulnar variance as the distance between the most distal aspect of the metaphysis of the radius and the ulna according to the Hafner distal-distal method (DIDI).
Time Frame
9 months
Title
Deformity
Description
Angulation in the oblique plane
Time Frame
2 weeks, 3 months and 9 months
Other Pre-specified Outcome Measures:
Title
Number of patients with anesthetic complications
Description
Number of participants with one of the following complications: Rash, pruritus, nausea, vomiting, bruising. hallucinations, toxicity, neurological injury, seizures, respiratory depression, bronchospasm, laryngospasm, cardiovascular events, malignant hyperthermia, and death.
Time Frame
During and immediately after the intervention
Title
Presence of a pressure ulcer (NPUAP scale)
Description
Pressure zones caused by plaster and classified with the National Pressure Ulcer Advisory Panel scale. The score range from 1 to 4. Higher scores mean a worse outcome. Unclassifiable lesions or those with deep tissue lesions will be reclassified to type 3 or 4 lesions after surgical debridement. For the purposes of the study, the value of the reclassification will be taken.
Time Frame
2 and 6 weeks
Title
Patients's pain control
Description
Days of analgesic consumption
Time Frame
2 and 6 weeks
Title
Number of patients with pin tract infection (Dahl scale)
Description
Only in patients with percutaneous fixation with K-wires will the pin tract infection be classified with the Dahl scale.
Time Frame
2 and 6 weeks
Title
Number of patients with reintervention
Description
Surgical intervention in the fractured radius during the nine months after the assigned treatment due to nonunion, re-displacement, or malunion
Time Frame
0 to 9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children from 5 years to 10 years Unilateral metaphyseal distal radius fracture Fracture shortening of 0 to 10mm or angulation of 10 ° to 20 ° in the oblique plane. (AO 23-M 2-3 or 23r-M 2-3) Admission in the first 14 days after the fracture Exclusion Criteria: Polytrauma: Injury Severity Score (ISS)> 16 Associated fracture in the same limb. Neuromuscular pathology (e.g., cerebral palsy, spinal muscular atrophy, Duchenne disease) Open fractures. History of fractures, septic arthritis, or osteomyelitis in the same limb. Neurological or vascular injury in the fractured upper limb. Known alteration of bone metabolism (e.g., osteogenesis imperfecta, rickets, osteopetrosis, skeletal dysplasias, lysosomal storage diseases). Congenital longitudinal deficiency.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maria F Garcia, MD
Phone
3534000
Email
m-garciar@javeriana.edu.co
First Name & Middle Initial & Last Name or Official Title & Degree
Julian D Rincon, MD
Phone
3534000
Ext
384
Email
jd.rincon@ioir.org.co
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria F Garcia, MD
Organizational Affiliation
Instituto Roosevelt
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto Roosevelt
City
Bogota
State/Province
Cundinamarca
ZIP/Postal Code
110321
Country
Colombia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria F Garcia, MD
Phone
3534000
Email
m-garciar@javeriana.edu.co

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Study information will be available through the institutional website.
IPD Sharing Time Frame
2 years
IPD Sharing Access Criteria
On permission request
IPD Sharing URL
https://www.institutoroosevelt.com
Citations:
PubMed Identifier
33709769
Citation
Marson BA, Ng JWG, Craxford S, Chell J, Lawniczak D, Price KR, Ollivere BJ, Hunter JB. Treatment of completely displaced distal radial fractures with a straight plaster or manipulation under anaesthesia. Bone Joint J. 2021 May;103-B(5):902-907. doi: 10.1302/0301-620X.103B.BJJ-2020-1740.R1. Epub 2021 Mar 12.
Results Reference
background
PubMed Identifier
35436224
Citation
Garcia-Rueda MF, Bohorquez-Penaranda AP, Gil-Laverde JFA, Aguilar-Sierra FJ, Mendoza-Pulido C. Casting Without Reduction Versus Closed Reduction With or Without Fixation in the Treatment of Distal Radius Fractures in Children: Protocol for a Randomized Noninferiority Trial. JMIR Res Protoc. 2022 Apr 14;11(4):e34576. doi: 10.2196/34576.
Results Reference
derived

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Immobilization Without Reduction vs. Reduction Under General Anesthesia in Metaphyseal Fractures of the Distal Radius

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