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Use of the Bioabsorbable Activa IM-Nail™ in Pediatric Diaphyseal Forearm Fractures

Primary Purpose

Fracture Fixation, Intramedullary, Forearm Fracture, Fracture Healing

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Activa IM-Nail
Sponsored by
Children's Fractures Interest Group, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fracture Fixation, Intramedullary

Eligibility Criteria

2 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Acute traumatic diaphyseal forearm fracture of the radius, ulna or both
  • Fractures need to be complete (not unicortical or green stick)
  • Displaced more than 50% of bone width or angulated more than 10° in any plane or irreducible or unstable after reduction

Exclusion Criteria:

We exclude patients

  • with fractures that are well managed conservatively (undisplaced or minimally displaced)
  • with previous ipsilateral forearm fracture
  • with fractures unsuited for intramedullary nailing (e.g. multifragmentary, metaphyseal or epiphyseal)
  • with fractures with ipsilateral wrist or elbow involvement (e.g. Monteggia or Galeazzi variants)
  • unable to participate in follow-up
  • with existing bone pathology (e.g. tumor, osteogenesis imperfecta, degenerative disease)
  • in whom internal fixation is otherwise contraindicated (e.g. active or potential infection)

Sites / Locations

  • Herlev and Gentofte University HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Activa IM-Nail

Arm Description

Activa IM-Nail

Outcomes

Primary Outcome Measures

Radiographic Union Score (RUS)
RUS is a score derived from assessing AP and lateral radiographs. Each bone cortex (anterior, posterior, medial and lateral) is assigned a score of 1 to 3. A cortex with a visible fracture line and no callus is given a score of 1, a cortex with callus but a visible fracture line is scored as 2 and a cortex with bridging callus and no visible fracture line is scored as 3. Scores are added to give a minimum score of 4 (definitely not healed) and a maximum of 12 (definitely healed). 12 is best.

Secondary Outcome Measures

Faces Pain Scale - Revised (FPS-R)
To measure the outcome of pain in children below 8 years of age. Pain evaluated by the child selecting 1 of 6 faces that represents their feeling of pain. Faces are scored 0, 2, 4, 6, 8 or 10. Scale 0-10 with 2 point increments. 0 = no pain, 10= very much pain. 0 is best.
Bilateral elbow and forearm range of motion
Measured in degrees by goniometer
Visual Analogue Scale (VAS)
Pain evaluated by the child putting a mark on a 10 cm long line. Most left=no pain, most right=worst possible pain. Distance from most left to the child's mark is measured with a ruler. 1 mm = 1 point. Value is given with 1 decimal, e.g. 64 mm = 6,4 points. Scale 0.0-10.0. With 0 = no pain, 10= worst possible pain. 0 is best.

Full Information

First Posted
May 24, 2021
Last Updated
June 23, 2021
Sponsor
Children's Fractures Interest Group, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT04941612
Brief Title
Use of the Bioabsorbable Activa IM-Nail™ in Pediatric Diaphyseal Forearm Fractures
Official Title
Use of the Bioabsorbable Activa IM-Nail™ in Pediatric Diaphyseal Forearm Fractures: a Cohort Study of 30 Patients
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Recruiting
Study Start Date
May 25, 2021 (Actual)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
May 25, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Fractures Interest Group, Denmark

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Background Pediatric diaphyseal forearm fractures are common and one of the most frequent reasons for orthopedic care. Fractures in need of surgery are often treated with metal Elastic Stable Intramedullary Nails (ESIN). Nail removal after 6-12 months is generally advocated. Surgical hardware removal has few complications; however, it is a substantial burden on the child, the family and healthcare economy. Bioabsorbable Intramedullary Nails (BIN) have been developed for the same indications as metal ESIN. The use of bioabsorbable implants would deem hardware removal unnecessary and relieve the child of further surgery and reduce healthcare costs. Methods The investigators aim to recruit all children in the catchment area of Herlev and Gentofte University Hospital (Copenhagen, Denmark) with acute unstable diaphyseal forearm fractures. Participants will be operated with BIN and followed consecutively for 2 years with interim analysis of data after 6 months. The investigators will report radiological healing using the Radiographic Union Score (RUS) 3 months after surgery together with any adverse events during follow-up. Discussion This study will provide important preliminary data and asses the feasibility of using the bioabsorbable Activa IM-Nail™ in pediatric diaphyseal forearm fractures. This study is a pilot study for initiating an RCT comparing BIN to metal ESIN hypothesizing that BIN is not an inferior treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fracture Fixation, Intramedullary, Forearm Fracture, Fracture Healing, Child, Only, Implant Complication

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Cohort study
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Activa IM-Nail
Arm Type
Experimental
Arm Description
Activa IM-Nail
Intervention Type
Device
Intervention Name(s)
Activa IM-Nail
Intervention Description
PLGA bioabsorbable intramedullary nail
Primary Outcome Measure Information:
Title
Radiographic Union Score (RUS)
Description
RUS is a score derived from assessing AP and lateral radiographs. Each bone cortex (anterior, posterior, medial and lateral) is assigned a score of 1 to 3. A cortex with a visible fracture line and no callus is given a score of 1, a cortex with callus but a visible fracture line is scored as 2 and a cortex with bridging callus and no visible fracture line is scored as 3. Scores are added to give a minimum score of 4 (definitely not healed) and a maximum of 12 (definitely healed). 12 is best.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Faces Pain Scale - Revised (FPS-R)
Description
To measure the outcome of pain in children below 8 years of age. Pain evaluated by the child selecting 1 of 6 faces that represents their feeling of pain. Faces are scored 0, 2, 4, 6, 8 or 10. Scale 0-10 with 2 point increments. 0 = no pain, 10= very much pain. 0 is best.
Time Frame
3 months
Title
Bilateral elbow and forearm range of motion
Description
Measured in degrees by goniometer
Time Frame
3 months
Title
Visual Analogue Scale (VAS)
Description
Pain evaluated by the child putting a mark on a 10 cm long line. Most left=no pain, most right=worst possible pain. Distance from most left to the child's mark is measured with a ruler. 1 mm = 1 point. Value is given with 1 decimal, e.g. 64 mm = 6,4 points. Scale 0.0-10.0. With 0 = no pain, 10= worst possible pain. 0 is best.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute traumatic diaphyseal forearm fracture of the radius, ulna or both Fractures need to be complete (not unicortical or green stick) Displaced more than 50% of bone width or angulated more than 10° in any plane or irreducible or unstable after reduction Exclusion Criteria: We exclude patients with fractures that are well managed conservatively (undisplaced or minimally displaced) with previous ipsilateral forearm fracture with fractures unsuited for intramedullary nailing (e.g. multifragmentary, metaphyseal or epiphyseal) with fractures with ipsilateral wrist or elbow involvement (e.g. Monteggia or Galeazzi variants) unable to participate in follow-up with existing bone pathology (e.g. tumor, osteogenesis imperfecta, degenerative disease) in whom internal fixation is otherwise contraindicated (e.g. active or potential infection)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Morten J Andersen, MD
Phone
004538681479
Email
mortenjonandersen@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Morten J Andersen, MD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Herlev and Gentofte University Hospital
City
Herlev
State/Province
Capital Region
ZIP/Postal Code
2730
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Morten J Andersen, MD
Phone
004538681479
Email
morten.jon.andersen@regionh.dk

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Use of the Bioabsorbable Activa IM-Nail™ in Pediatric Diaphyseal Forearm Fractures

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