Plate Osteosynthesis Versus ESIN of Displaced Midclavicular Fractures

NCT ID: NCT01015924

Last Updated: 2014-01-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2/PHASE3

Total Enrollment

125 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-07-31

Study Completion Date

2013-09-30

Brief Summary

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The purpose of this study is to compare two widely used operative techniques on displaced midshaft clavicular fractures. The hypothesis is that there is no difference in functional outcome.

Detailed Description

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Clavicular fracture is one of the most common fractures, accounting for about 4 % of all fractures. Midshaft fractures account for approximately 80%. Traditionally, midshaft fractures have been thought to have a good prognosis even when substantially displaced, and most have been treated nonoperatively with a sling or a figure of eight bandage. Early studies by Neer and Rowe in the 60´s demonstrated a very low non-union rate, with av prevalence of 4 in a series of 566 patients, and 3 nonunions in 2235 in another. On this basis, the general view has been that the vast majority of even severely displaced midshaft fractures healed uneventfully, with a very low nonunion rate and a good functional result. Operative results reported on the other hand bad results, especially concerning the risk of infection. Recent studies, however, conclude differently, and suggest the outcomes of displaced fractures might not be as favourable as once thought. Hill showed in a series of 52 completely displaced midclavicular fractures a nonunion rate of 15% (8 of 52 patients) and 31% (16 of 52) of patients were not satisfied with the end result. This correlated with a shortening of more than 2 cm. In a prospective study of 222 patients by Nowak, 42% (93 of 222) were found to have persisting symptoms after 6 months wheras 15% were found to have nonunion. These symptoms seem to persist even after 9 - 10 years reporting 29 % of 208 patients having pain during activity and 9% pain at rest. 46% did not consider themselves fully recovered.

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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Clavicle Fractures

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

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

Group Type ACTIVE_COMPARATOR

plate osteosynthesis

Intervention Type PROCEDURE

Patients are operated upon within 3 w of the fracture

ESIN

Intervention Type PROCEDURE

Elastiv stable intramedullary nailing

Plate osteosynthesis

Open reduction and plate fixation of midshaft clavicle fractures

Group Type ACTIVE_COMPARATOR

plate osteosynthesis

Intervention Type PROCEDURE

Patients are operated upon within 3 w of the fracture

ESIN

Intervention Type PROCEDURE

Elastiv stable intramedullary nailing

Interventions

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plate osteosynthesis

Patients are operated upon within 3 w of the fracture

Intervention Type PROCEDURE

ESIN

Elastiv stable intramedullary nailing

Intervention Type PROCEDURE

Other Intervention Names

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The standard plate i a precontoured LCP clavicle plate by Synthes TEN, synthes

Eligibility Criteria

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Inclusion Criteria

1. 16 - 60 years of age
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

1. More than 4 weeks old fracture
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
Minimum Eligible Age

16 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Akershus

OTHER

Sponsor Role lead

Responsible Party

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Hendrik Frolich Fuglesang

Assistant Prof. Stein Erik Utvåg, MD, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status

Countries

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Norway

Other Identifiers

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rek 1.2009.1196

Identifier Type: -

Identifier Source: org_study_id

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