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A Randomized Trial Comparing Conventional Plaster and Thermoplastic Splints to Treat Pediatric Boxer's Fractures

Primary Purpose

Bone Fractures, Splints, Metacarpal Fracture

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Plaster Ulnar Gutter Splint
Thermoplastic Splint
Sponsored by
IWK Health Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bone Fractures focused on measuring boxer's fracture, metacarpal neck fracture, metacarpal fracture

Eligibility Criteria

undefined - 16 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Isolated 5th metacarpal neck fracture
  • Less than 10 days from injury

Exclusion Criteria:

  • Multiple Metacarpal fractures
  • Significant injuries to other hand structures (tendons, nerves, major arteries)

Sites / Locations

  • IWK Health Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Plaster Ulnar Gutter Splint

Thermoplastic Splint

Arm Description

Patients will have their hand placed in a conventional Plaster ulnar gutter splint. This immobilizes all joints of the ring and small fingers and the wrist

Patients will be fitted with a custom molded thermoplastic splint that stabilizes the metacarpals of the injured hand but does not immobilize any joints

Outcomes

Primary Outcome Measures

Range of Motion
The active and passive Range of Motion (ROM) will be tested at 3 time points, for all fingers and the wrist
Compliance
The compliance rate of subjects in each group wearing the splint at all times for the prescribed duration (3 weeks) will be assessed.

Secondary Outcome Measures

Pain
Pain, reported on a Visual Analog Scale, will be assessed at specified time points
Complications
Loss of fracture reduction, malunion or non-union will be monitored throughout the study
Validated Outcome Questionnaire
Patients will complete the Pediatric Outcomes Data Collection Instrument (PODCI) at several time points
Grip Strength
Patients will have their grip strength measured for the injured and non-injured hand at 6 and 12 weeks post fracture
Radiographic assessment of fracture
An X-ray of the injured had will be done in 3 views. This will be assessed by one of the investigators, in a blinded fashion. They will determine the angulation and assess for evidence of bony healing

Full Information

First Posted
December 30, 2012
Last Updated
January 12, 2016
Sponsor
IWK Health Centre
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1. Study Identification

Unique Protocol Identification Number
NCT01759758
Brief Title
A Randomized Trial Comparing Conventional Plaster and Thermoplastic Splints to Treat Pediatric Boxer's Fractures
Official Title
Conventional Plaster Versus Thermoplastic Splint for the Treatment of a Pediatric Metacarpal Neck Fracture: a Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
December 2012 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
June 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IWK Health Centre

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators are conducting a randomized clinical trial comparing two types of splints for treatment of Boxer's fractures in children up to age 17 inclusive. Patients who meet inclusion criteria will be randomized to either Group A or B. Group A will be treated with the conventional plaster ulnar gutter splint. Group B will be treated with a custom molded thermoplastic hand-based splint. The thermoplastic splint will provide support of the metacarpal but does not immobilize the patient's wrist or interphalangeal joints. Hypothesis: Is plaster splint immobilization an equivalent treatment method to a custom made thermoplastic splint for a fifth metacarpal neck fracture? Will one splint be tolerated better than the other and will the compliance be different between the two groups?
Detailed Description
Nearly all Boxer's fractures are treated without surgery using a splint to keep part or all of the hand from moving (immobilization). There are several acceptable methods of immobilization used by hand surgeons, using splints of different sizes and materials for variable periods of time(1-6). A recent systematic review from The Cochrane Collaboration found the current data to be inconclusive with regards to the optimal immobilization technique and highlighted the need for further studies(2). Specifically, it was recommended that future studies include functional outcome measures, timing of return to work, complications, pain scores, and an economic analysis. The current practice at the investigators' institution is for patients to be splinted in a plaster ulnar gutter splint, in the Emergency Department and referred to the next available plastic surgery clinic. If needed, a closed reduction would be performed in clinic, if there was a significant angulation (greater than 45 degrees) or any clinical rotation deformity. The most common method of immobilization involves placing the wrist, ring finger and little finger all the way from the fingertips to the mid-forearm in molded plaster called an ulnar gutter splint. The splint is left on 24 hours a day for 3 to 4 weeks and then removed in the clinic. Many patients find it difficult to keep the splint on for the full 3 to 4 weeks for a number of reasons. The plaster needs to stay dry, making it awkward to bathe. The splint can also get loose and rub as the swelling around the fracture gets better. The splint can also start to smell because sweat builds up under it. Some patients find the plaster material heavy, making it difficult to wear. Finally, many patients are self-conscious about the appearance of the splint and remove it for this reason alone. In the investigators' experience, up to 1 out of 5 patients will remove the splint on their own against doctor's orders for one reason or another. When patients do follow instructions and keep the splint on 24 hours a day for 3 to 4 weeks, this can lead to joint stiffness when the splint is removed. Some patients may even require physiotherapy to regain their normal finger movement and grip strength. It is unknown if the ulnar gutter splint is really the best way to immobilize the hand after a Boxer's fracture. It is unknown what material is best for making the splint, whether it is truly necessary to keep the entirety of the wrist and ring and little fingers still, and for how long the hand and fingers should be kept still. Most surgeons recommend patients wear a splint for 3 to 4 weeks. The investigators would like to determine if a smaller splint made of more durable, lighter moldable plastic that allows earlier movement of the hand and fingers while still keeping the fracture from moving gives the same result as the commonly used ulnar gutter splint. Functional Hand Based Splint (Thermoplastic Splint) The functional hand-based splint is made of custom molded hard plastic and is fitted over the hand only. A thermoplastic splint is made from plastic that is heated and custom-fitted to the subject's hand, which hardens when it cools. This thermoplastic splint is custom fitted by an occupational therapist such that all joints are free to move. The splint does not limit the patient from moving their wrist or fingers while wearing it. It is custom molded such that it fits snuggly over the patient's hand and holds the fracture in a stable position. Several adult studies have found this type of custom molded splint superior to either surgical treatment and/or plaster splint immobilization because it resulted in less stiffness, better movement after splint removal, and no increased pain (4-7). The investigators are not aware of any comparative studies done in pediatric patients. Compliance Patient compliance for wearing their splint for the prescribed during can be a problem. At the investigators' institution, there is a non-compliance rate of approximately 15 to 20 % for Boxer's fracture patients. The investigators hypothesize that the hand-based splint will be better tolerated by patients and therefore result in a higher rate of compliance for the prescribed duration that the plaster splint. Also, the thermoplastic splint will not be damaged if it gets wet, which may translate into fewer additional visits to the clinic or emergency department to have the splint replaced. This study will be a randomized, single-blinded controlled trial. The randomization of the two splint types will be determined by a computer-based number generator. The patients will know what type of splint they have, but the plastic surgeons and physiotherapist who examine and test the subjects ROM and grip strength will not know the type of splint for each subject. Patients will be randomized to one of the two groups at their first clinic visit, within 7 days of their injury. They will have their splint placed at this visit and are to wear the splint at all times for 3 weeks. Subjects will return to clinic at 1, 3, 6, and 12 weeks to be reassessed. Specified outcome measures (primary and secondary) will be tested at each visit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bone Fractures, Splints, Metacarpal Fracture, Boxer's Fracture
Keywords
boxer's fracture, metacarpal neck fracture, metacarpal fracture

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Plaster Ulnar Gutter Splint
Arm Type
Active Comparator
Arm Description
Patients will have their hand placed in a conventional Plaster ulnar gutter splint. This immobilizes all joints of the ring and small fingers and the wrist
Arm Title
Thermoplastic Splint
Arm Type
Experimental
Arm Description
Patients will be fitted with a custom molded thermoplastic splint that stabilizes the metacarpals of the injured hand but does not immobilize any joints
Intervention Type
Other
Intervention Name(s)
Plaster Ulnar Gutter Splint
Other Intervention Name(s)
Conventional Plaster splint, Plaster of Paris
Intervention Description
Patients are placed in a plaster ulnar gutter splint, molded in the safe position.
Intervention Type
Other
Intervention Name(s)
Thermoplastic Splint
Other Intervention Name(s)
Functional brace, Moulded brace, Moulded Metacarpal brace
Intervention Description
Thermoplastic Splint is heat moulded to the patient's hand, stabilizing the metacarpal heads, but not immobilizing any joints. This is done by our occupational therapist.
Primary Outcome Measure Information:
Title
Range of Motion
Description
The active and passive Range of Motion (ROM) will be tested at 3 time points, for all fingers and the wrist
Time Frame
up to 12 weeks
Title
Compliance
Description
The compliance rate of subjects in each group wearing the splint at all times for the prescribed duration (3 weeks) will be assessed.
Time Frame
3 weeks post fracture
Secondary Outcome Measure Information:
Title
Pain
Description
Pain, reported on a Visual Analog Scale, will be assessed at specified time points
Time Frame
1, 3, 6, and 12 weeks post fracture
Title
Complications
Description
Loss of fracture reduction, malunion or non-union will be monitored throughout the study
Time Frame
3, 6, and 12 weeks
Title
Validated Outcome Questionnaire
Description
Patients will complete the Pediatric Outcomes Data Collection Instrument (PODCI) at several time points
Time Frame
3, 6, and 12 weeks
Title
Grip Strength
Description
Patients will have their grip strength measured for the injured and non-injured hand at 6 and 12 weeks post fracture
Time Frame
6 and 12 weeks
Title
Radiographic assessment of fracture
Description
An X-ray of the injured had will be done in 3 views. This will be assessed by one of the investigators, in a blinded fashion. They will determine the angulation and assess for evidence of bony healing
Time Frame
12 weeks post fracture

10. Eligibility

Sex
All
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Isolated 5th metacarpal neck fracture Less than 10 days from injury Exclusion Criteria: Multiple Metacarpal fractures Significant injuries to other hand structures (tendons, nerves, major arteries)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Bezuhly, MD, MSc, SM
Organizational Affiliation
Assistant Professor, Clinician-Investigator at IWK Health Centre and Dalhousie University
Official's Role
Principal Investigator
Facility Information:
Facility Name
IWK Health Centre
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3K6R8
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
4247878
Citation
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16034891
Citation
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Results Reference
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PubMed Identifier
9659472
Citation
Braakman M, Oderwald EE, Haentjens MH. Functional taping of fractures of the 5th metacarpal results in a quicker recovery. Injury. 1998 Jan;29(1):5-9. doi: 10.1016/s0020-1383(97)00106-x.
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PubMed Identifier
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Citation
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PubMed Identifier
10505445
Citation
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PubMed Identifier
14639483
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Results Reference
derived

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A Randomized Trial Comparing Conventional Plaster and Thermoplastic Splints to Treat Pediatric Boxer's Fractures

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