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Conservative Interventions for Treating Clavicle Fractures in Adults

Primary Purpose

Fracture of Clavicle

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
a standard arm sling
a figure-of-eight bandage
Sponsored by
Hospital Israelita Albert Einstein
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fracture of Clavicle focused on measuring Clavicle [mh], Fracture Healing [mh], Fractures, Bone [mh], Treatment outcome [mh], Conservative treatment [tw]

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adults aged 18 years or older and 65 years or less with middle third clavicle fracture,
  • Acute fracture (less than 10 days), we will include all types of middle third clavicle fractures (non-displaced and displaced fractures),
  • No medical contraindication to proposed methods of immobilisation,
  • Understanding of Portuguese language and written informed consent.

Exclusion Criteria:

  • Pathological fracture,
  • Open fracture,
  • Neurovascular injury on physical examination,
  • Associated head injury (Glasgow Coma Scale score of <12),
  • Ipsilateral upper limb fractures and/or dislocation(except hand and fingers),
  • History of frozen shoulder,
  • Previous disease in the limb that could influence the results (e.g. rheumatoid arthritis),
  • Inability to comply with follow-up (inability to read or complete forms).

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Group 1: a standard arm sling

    Group 2: a figure-of-eight bandage

    Arm Description

    Group 1: the orthopaedic surgeon will apply a standard arm sling that will be used for four weeks; however, during these weeks, participants will be encouraged to discard the sling when their pain has subsided. After four weeks the same orientations of group 1 will be done to this group.

    Group 2: a figure-of-eight bandage will be used for four weeks, and every week the participants will return to check and adjust the immobilisation. In this way, the dominant hand can remain free and simple activities will be allowed (writing, keyboarding and other). After four weeks, participants will be encouraged to discard the bandage, but load bearing will not be allowed before osseous consolidation (around 10 weeks).

    Outcomes

    Primary Outcome Measures

    Function or disability will be measured by DASH - Disability of the Arm, Shoulder, and Hand questionnaire
    Function or disability will be measured by DASH - Disability of the Arm, Shoulder, and Hand questionnaire validated and translated into Portuguese in Brazil, the final score of the DASH questionnaire will be converted to a percentage via the following formula: Scoring = [Sum of answers n/n - 1] X 25, where n is the number of complete answers. The two optional modules will not be measured. The value obtained will be directly proportional to the percentage of impairment of the limb function.

    Secondary Outcome Measures

    Modified University of California at Los Angeles (modified - UCLA)
    Modified University of California at Los Angeles (modified - UCLA), validated and translated into Portuguese in Brazil.
    Pain measured on a 0 to 100 using visual analogue scale (VAS)
    Pain measured on a 0 to 100 using visual analogue scale (VAS) (with 0 indicating no pain and 100 indicating the maximum pain). As reported in the literature, a clinically important change will be considered as a 30% or more change in pain score.
    Treatment failure measured by the number of participants who have undergone or are being considered a surgical intervention
    Treatment failure measured by the number of participants who have undergone or are being considered a surgical intervention (e.g. symptomatic non-union or malunion with intractable pain). Although studies evaluating patients with fractures without displacement reported low rates of nonunion (about 0.03%), studies with patients with displaced fractures found nonunion rates of up to 15%. Therefore, we expect between 5 and 10% of our participants might provide symptomatic nonunion during follow-up. Patients who experience this complication during follow-up study will be treated surgically with open reduction and internal fixation with pre-contoured locking plate counted down the superior surface of the clavicle and bone grafting when necessary.
    Adverse events
    Adverse events measured by: a) Cosmetic result: perception of deformity or asymmetric result (dichotomous data); b) Asymptomatic non-union (i.e. the fracture has not healed radiographically with no pain); c) Stiffness/restricted of range of shoulder movement (compared with contralateral side).
    Numbers returning to previous activities (work, sport, activities of daily living), including time to return.
    Numbers returning to previous activities (work, sport, activities of daily living), including time to return.

    Full Information

    First Posted
    March 12, 2015
    Last Updated
    March 19, 2015
    Sponsor
    Hospital Israelita Albert Einstein
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02398006
    Brief Title
    Conservative Interventions for Treating Clavicle Fractures in Adults
    Official Title
    Figure-of-eight Bandage Versus Arm Sling for Treating Middle Third Clavicle Fractures in Adults: Study Protocol for a Randomised Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2015
    Overall Recruitment Status
    Unknown status
    Study Start Date
    April 2015 (undefined)
    Primary Completion Date
    September 2016 (Anticipated)
    Study Completion Date
    December 2017 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Hospital Israelita Albert Einstein

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Background: Fracture of the clavicle is common accounting for 2.6% to 4 % of all fractures, with an overall incidence of 36.5 to 64 per 100,000 per year. Around 80% of clavicle fractures occur in the middle third of the clavicle. There is a lack of evidence of randomised controlled trials assessing the best treatment of these fractures. The objective of this study is to evaluate the effects (benefits and harms) of conservative interventions: figure-of-eight bandage versus sling for the treating middle third clavicle fractures. Methods/Design: this project has been designed as a single-centre, parallel-group randomised controlled trial that will compare figure-of-eight bandage versus sling. The investigators aim to recruit 110 adults, aged 18 years or older, with an acute (less than 10 days) middle third clavicle fracture. Primary outcomes will be function or disability measured by DASH questionnaire; the secondary outcomes will be: modified UCLA score pain, treatment failure, adverse events and numbers returning to previous activities. Data analysis: the chi-square test will be used to analyse the results of categorical variables, and Student t-test will be used to compare groups with respect to the numerical variables. The Student t-test is used to compare the clinical outcome of each group at 1, 2 and 4 weeks and at 6 and 12 months after the intervention. The significance level of 5% (alpha = 0.05) is used for all statistical tests such that tests have a value of less than 0.05 are considered statistically significant. Discussion: According to current evidence there is very limited evidence from two single trials only regarding the effectiveness of different methods of conservative interventions for treating clavicle fractures. This study is one of the first randomised controlled trials following the CONSORT statements designed to compare two conservative methods for treating clavicle fractures (figure-of-eight versus sling).
    Detailed Description
    Whilst there are several options for conservative treatment for middle third clavicle fractures, only two randomised controlled published in the 80s attempted to determine the effects of different methods for conservative treatment for middle third clavicle fractures. Thus, a pragmatic trial design has been chosen as it can directly inform clinical practice; our inclusion criteria will reflect the variety in patient presentations that would be encountered by general orthopaedic surgeons in the clinical setting. The current trial includes design characteristics known to minimise bias. Participants will be assigned using a concealed random procedure, assessments and data analysis will be blinded and we will use the intention-to-treat analysis.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Fracture of Clavicle
    Keywords
    Clavicle [mh], Fracture Healing [mh], Fractures, Bone [mh], Treatment outcome [mh], Conservative treatment [tw]

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    110 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Group 1: a standard arm sling
    Arm Type
    Active Comparator
    Arm Description
    Group 1: the orthopaedic surgeon will apply a standard arm sling that will be used for four weeks; however, during these weeks, participants will be encouraged to discard the sling when their pain has subsided. After four weeks the same orientations of group 1 will be done to this group.
    Arm Title
    Group 2: a figure-of-eight bandage
    Arm Type
    Active Comparator
    Arm Description
    Group 2: a figure-of-eight bandage will be used for four weeks, and every week the participants will return to check and adjust the immobilisation. In this way, the dominant hand can remain free and simple activities will be allowed (writing, keyboarding and other). After four weeks, participants will be encouraged to discard the bandage, but load bearing will not be allowed before osseous consolidation (around 10 weeks).
    Intervention Type
    Other
    Intervention Name(s)
    a standard arm sling
    Intervention Description
    Closed reduction (re-aligning the fragments of the fracture) will be not performed because the reduced position is practically impossible to maintain.
    Intervention Type
    Other
    Intervention Name(s)
    a figure-of-eight bandage
    Intervention Description
    Closed reduction (re-aligning the fragments of the fracture) will be not performed because the reduced position is practically impossible to maintain.
    Primary Outcome Measure Information:
    Title
    Function or disability will be measured by DASH - Disability of the Arm, Shoulder, and Hand questionnaire
    Description
    Function or disability will be measured by DASH - Disability of the Arm, Shoulder, and Hand questionnaire validated and translated into Portuguese in Brazil, the final score of the DASH questionnaire will be converted to a percentage via the following formula: Scoring = [Sum of answers n/n - 1] X 25, where n is the number of complete answers. The two optional modules will not be measured. The value obtained will be directly proportional to the percentage of impairment of the limb function.
    Time Frame
    12 months
    Secondary Outcome Measure Information:
    Title
    Modified University of California at Los Angeles (modified - UCLA)
    Description
    Modified University of California at Los Angeles (modified - UCLA), validated and translated into Portuguese in Brazil.
    Time Frame
    12 months
    Title
    Pain measured on a 0 to 100 using visual analogue scale (VAS)
    Description
    Pain measured on a 0 to 100 using visual analogue scale (VAS) (with 0 indicating no pain and 100 indicating the maximum pain). As reported in the literature, a clinically important change will be considered as a 30% or more change in pain score.
    Time Frame
    12 months
    Title
    Treatment failure measured by the number of participants who have undergone or are being considered a surgical intervention
    Description
    Treatment failure measured by the number of participants who have undergone or are being considered a surgical intervention (e.g. symptomatic non-union or malunion with intractable pain). Although studies evaluating patients with fractures without displacement reported low rates of nonunion (about 0.03%), studies with patients with displaced fractures found nonunion rates of up to 15%. Therefore, we expect between 5 and 10% of our participants might provide symptomatic nonunion during follow-up. Patients who experience this complication during follow-up study will be treated surgically with open reduction and internal fixation with pre-contoured locking plate counted down the superior surface of the clavicle and bone grafting when necessary.
    Time Frame
    12 months
    Title
    Adverse events
    Description
    Adverse events measured by: a) Cosmetic result: perception of deformity or asymmetric result (dichotomous data); b) Asymptomatic non-union (i.e. the fracture has not healed radiographically with no pain); c) Stiffness/restricted of range of shoulder movement (compared with contralateral side).
    Time Frame
    12 months
    Title
    Numbers returning to previous activities (work, sport, activities of daily living), including time to return.
    Description
    Numbers returning to previous activities (work, sport, activities of daily living), including time to return.
    Time Frame
    12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Adults aged 18 years or older and 65 years or less with middle third clavicle fracture, Acute fracture (less than 10 days), we will include all types of middle third clavicle fractures (non-displaced and displaced fractures), No medical contraindication to proposed methods of immobilisation, Understanding of Portuguese language and written informed consent. Exclusion Criteria: Pathological fracture, Open fracture, Neurovascular injury on physical examination, Associated head injury (Glasgow Coma Scale score of <12), Ipsilateral upper limb fractures and/or dislocation(except hand and fingers), History of frozen shoulder, Previous disease in the limb that could influence the results (e.g. rheumatoid arthritis), Inability to comply with follow-up (inability to read or complete forms).
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Mario Lenza, PhD
    Phone
    55 11 21511444
    Email
    mario.lenza@einstein.br
    First Name & Middle Initial & Last Name or Official Title & Degree
    Mario Ferretti, PhD
    Phone
    55 11 21511444
    Email
    ferretti@einstein.br
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Mario Lenza, PhD
    Organizational Affiliation
    Hospital Israelita Albert Einstein
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    27142768
    Citation
    Lenza M, Taniguchi LF, Ferretti M. Figure-of-eight bandage versus arm sling for treating middle-third clavicle fractures in adults: study protocol for a randomised controlled trial. Trials. 2016 May 4;17(1):229. doi: 10.1186/s13063-016-1355-8.
    Results Reference
    derived

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