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Sup-ER Protocol RCT

Primary Purpose

Birth Related Brachial Plexus Injury, Obstetrical Brachial Plexus Palsy

Status
Terminated
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Sup-ER Protocol
Control
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Birth Related Brachial Plexus Injury focused on measuring birth related brachial plexus injury, brachial plexus, splint

Eligibility Criteria

6 Weeks - 8 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of brachial plexus injury at birth.
  • Significant deficit in external rotation and/or supination of the affected limb based on clinical assessment using the Toronto Active Movement Scale at 6 weeks of age (External Rotation ≤ 2 and/or Supination ≤ 2)
  • Tightness in Passive Range of Motion of external rotation: any angle of less than 180°.
  • Age 6-8 weeks

Exclusion Criteria:

  • Neuromuscular disorder
  • Unwillingness or inability to comply with the requirements of the study protocol.

Sites / Locations

  • BC Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Sup-ER protocol

Control

Arm Description

Early shoulder repositioning (Sup-ER Splint)

Standard treatment

Outcomes

Primary Outcome Measures

Toronto Active Movement Scale

Secondary Outcome Measures

Full Information

First Posted
August 28, 2013
Last Updated
November 14, 2017
Sponsor
University of British Columbia
Collaborators
Children's & Women's Health Centre of British Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT01933438
Brief Title
Sup-ER Protocol RCT
Official Title
Does Early Supination and External Rotation Repositioning in Children With Birth Related Brachial Plexus Injury Have Benefit? A Randomized Controlled Trial of the Sup-ER Protocol.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Terminated
Why Stopped
The study ended early after encountering logistics challenges and difficulties with site recruitment.
Study Start Date
June 2013 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of British Columbia
Collaborators
Children's & Women's Health Centre of British Columbia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study evaluates the ability of a supination and external rotation protocol to improve the arm function and anatomy of children with birth related brachial plexus injuries.
Detailed Description
The brachial plexus is a group of 5 nerves from the spinal cord that provide the movement and sensation of an upper extremity. In some difficult deliveries, traction on the shoulder may lead to damage to the brachial plexus and will result in an arm that is paralyzed. This is called 'birth related brachial plexus injury' (BRBPI). This may occur in up to 1/1000 births and the nerves may be injured minimally to severely. About 2/3 of children with this injury will recover to quite functional levels simply by maintaining looseness of joints while their nerves slowly heal. Some children have nerve injuries severe enough that they require surgical reconstruction with nerve grafts and nerve transfers to achieve even adequate function. Even in children with otherwise "good" recovery, the motions of external rotation of the shoulder and supination of the forearm are weaker, later to recover, and often incomplete. More importantly, lack of full motion leads to long term changes in the structure, growth, and posture of the shoulder requiring further musculoskeletal surgery, or a child with permanent deformity or disability. Any gains in active and passive range of motion during the first year of life may improve these long-term shoulder outcomes. The investigators have instituted a program of early passive repositioning mostly using a custom Sup-ER (Supination and External Rotation) splint during early growth and development to improve arm position and range of motion where ER and Sup are weak. In compliant patients in a pilot study, the speed and strength of recovery of ER and Supination are improved compared to historical controls. It is a novel splint and protocol designed by the investigators. This study is a randomized controlled trial to evaluate the use of the Sup-ER protocol in multiple centres over a two year period by assessing the arm function at common time points in recovery. The subjects are randomized to the Sup-ER protocol or the currently accepted standard treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Birth Related Brachial Plexus Injury, Obstetrical Brachial Plexus Palsy
Keywords
birth related brachial plexus injury, brachial plexus, splint

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sup-ER protocol
Arm Type
Experimental
Arm Description
Early shoulder repositioning (Sup-ER Splint)
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Standard treatment
Intervention Type
Other
Intervention Name(s)
Sup-ER Protocol
Intervention Description
Early shoulder repositioning (Sup-ER Splint)
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Standard treatment
Primary Outcome Measure Information:
Title
Toronto Active Movement Scale
Time Frame
1 year of age

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Weeks
Maximum Age & Unit of Time
8 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of brachial plexus injury at birth. Significant deficit in external rotation and/or supination of the affected limb based on clinical assessment using the Toronto Active Movement Scale at 6 weeks of age (External Rotation ≤ 2 and/or Supination ≤ 2) Tightness in Passive Range of Motion of external rotation: any angle of less than 180°. Age 6-8 weeks Exclusion Criteria: Neuromuscular disorder Unwillingness or inability to comply with the requirements of the study protocol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cynthia Verchere, MD FRCSC
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
BC Children's Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6H 3V4
Country
Canada

12. IPD Sharing Statement

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Sup-ER Protocol RCT

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