Plate Osteosynthesis Versus ESIN of Displaced Midclavicular Fractures

January 30, 2014 updated by: Hendrik Frolich Fuglesang, University Hospital, Akershus

Intramedullary Nailing Compared With Plate Fixation of Displaced Mid-clavicular Fractures. A Prospective Randomized Controlled Trial

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.

Study Overview

Status

Completed

Conditions

Detailed Description

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.

Study Type

Interventional

Enrollment (Actual)

125

Phase

  • Phase 2
  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Akershus
      • Lørenskog, Akershus, Norway, 1478
        • Akershus University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 60 years (ADULT, CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
ACTIVE_COMPARATOR: Elastic Stable Intramedullary Nailing
Operative intervention with closed or open reduction and intramedullary stabilization of midshaft clavicle fractures
Patients are operated upon within 3 w of the fracture
Other Names:
  • The standard plate i a precontoured LCP clavicle plate by Synthes
Elastiv stable intramedullary nailing
Other Names:
  • TEN, synthes
ACTIVE_COMPARATOR: Plate osteosynthesis
Open reduction and plate fixation of midshaft clavicle fractures
Patients are operated upon within 3 w of the fracture
Other Names:
  • The standard plate i a precontoured LCP clavicle plate by Synthes
Elastiv stable intramedullary nailing
Other Names:
  • TEN, synthes

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Functional outcome using DASH score
Time Frame: quick dash w 1 thru 6. DASH at 6, 12, 26, 52
quick dash w 1 thru 6. DASH at 6, 12, 26, 52

Secondary Outcome Measures

Outcome Measure
Time Frame
At each control, complication such as infection, thoracic outlet syndrome is evaluated
Time Frame: continuously, as well as w 6, 12, 26, 52
continuously, as well as w 6, 12, 26, 52
Constant score
Time Frame: evaluated 6w, 12w, 26w 52 w
evaluated 6w, 12w, 26w 52 w
SF 36
Time Frame: 26 w and 52 w
26 w and 52 w

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Stein Erik Utvag, MD PhD, University of Oslo

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2009

Primary Completion (ACTUAL)

September 1, 2013

Study Completion (ACTUAL)

September 1, 2013

Study Registration Dates

First Submitted

November 17, 2009

First Submitted That Met QC Criteria

November 17, 2009

First Posted (ESTIMATE)

November 18, 2009

Study Record Updates

Last Update Posted (ESTIMATE)

January 31, 2014

Last Update Submitted That Met QC Criteria

January 30, 2014

Last Verified

January 1, 2014

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • rek 1.2009.1196

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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