Plate Osteosynthesis Versus ESIN of Displaced Midclavicular Fractures
NCT ID: NCT01015924
Last Updated: 2014-01-31
Study Results
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Basic Information
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COMPLETED
PHASE2/PHASE3
125 participants
INTERVENTIONAL
2009-07-31
2013-09-30
Brief Summary
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Detailed Description
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Similar result were found in a systemic review of 2144 fractures. 15.1 % (24 of 159) of nonoperative treated dislocated fractures resulted in nonuion, whereas 2,2% (10 of 460) and 2% (5 of 152) nonunions were found in fractures treated operatively with either plate or intramedullary pins. On this basis, it is becoming more evident that conservative treatment gives much inferior results compared to earlier reported results.
The operative approach to midclavicular fractures have traditionally been plate osteosynthesis or intramedullary nailing. Poigenfürst in 1992 showed in a series of 122 patients a low nonunion rate and good functional results after plating. Likewise, intramedullary nailing has been described as an alternative technique with good results. Kettler demonstrated en a series of 87 patients a good functional results union in 97,7 % ( 85 of 87) and no infections. Similar results were fond by Rehm in 2004, with one nonunion of 136 fractures treated and a constant score one year after implant removal of 97.
Operative treatment of displaced midclavicular fracture thus shows reliable good results compared to earlier reported results. In 2007, the Canadian Orthopedic Trauma Society published a prospective randomised controlled trial of 132 patients, randomised to either conservative treatment with a sling, or plate fixation. The operative group showed clear superiority in Constant and DASH scores, reduction in risk of developing non-union, earlier return to work. With intramedullary nailing using ESIN technique, Smekal et al demonstrated superior results in the operative group in a prospective randomised controlled trial of 60 patients. 30 patients were opereated with elastic stable intramedullary nailing, and 30 patients were randomised to conservative treatment with a sling. The operative group had fewer complications, shorter time to union and a better functional outcome.
It seems from the above, that it is reasonable to offer operative treatment to active adults with displaced fractures of the middle third of the clavicle due to the risk of developing a symptomatic non- or malunion. Both plate fixation and intramedullary nailing of displaced fractures are described as safe methods of operative treatment. To our knowledge, there has never been conducted a prospective randomised controlled trial that compares different forms of the former mentioned operative alternatives.
On this basis, we plan to contuct a prospective randomised controlled trial comparing operative plate fixation and intramedullary nailing with TEN.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Elastic Stable Intramedullary Nailing
Operative intervention with closed or open reduction and intramedullary stabilization of midshaft clavicle fractures
plate osteosynthesis
Patients are operated upon within 3 w of the fracture
ESIN
Elastiv stable intramedullary nailing
Plate osteosynthesis
Open reduction and plate fixation of midshaft clavicle fractures
plate osteosynthesis
Patients are operated upon within 3 w of the fracture
ESIN
Elastiv stable intramedullary nailing
Interventions
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plate osteosynthesis
Patients are operated upon within 3 w of the fracture
ESIN
Elastiv stable intramedullary nailing
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Dislplaced midshaft clavicular fractures with no cortical bone contact or shortening over 15 mm
3. Tenting/compromised skin
4. Axial malalignment over 30 degrees
Exclusion Criteria
2. Ipsilateral damage that will influence the recovery and scoring systems, ie. Rotator cuff injury/fracture
3. Pathological fracture
4. Neurovascular injury
5. Open fracture
6. Noncompliance
7. Congenital anomaly or bone disease
8. Ongoing infectious process around the incision site for plate osteosynthesis
16 Years
60 Years
ALL
No
Sponsors
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University Hospital, Akershus
OTHER
Responsible Party
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Hendrik Frolich Fuglesang
Assistant Prof. Stein Erik Utvåg, MD, PhD
Principal Investigators
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Stein Erik Utvag, MD PhD
Role: STUDY_DIRECTOR
University of Oslo
Locations
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Akershus University Hospital
Lørenskog, Akershus, Norway
Countries
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Other Identifiers
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rek 1.2009.1196
Identifier Type: -
Identifier Source: org_study_id
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