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A biomechanical study on functional outcome after a midshaft clavicular fracture with a 3D- Electromagnetic Motion Tracking Device

A biomechanical study on functional outcome after a midshaft clavicular fracture with a 3D- Electromagnetic Motion Tracking Device - Biomechanics Clavicle Study (BMCS)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35922
Enrollment
32
Registered
2011-10-10
Start date
2011-12-20
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

clavicular fractures collar bone fractures

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • A (dislocated) midshaft clavicular fracture 1 or 5 years ago. • Age at time of fracture between 18 and 60 years. • Clavicular shortening of respectively, 20 mm. • Willingness to undergo functional tests with both arms.

Exclusion criteria

Exclusion criteria: • Current or previous fracture in the proximal or distal third of the clavicle, or acromio-clavicular injury. • Prior surgery to the shoulder or prior shoulder complaints before fracture. • Neurovascular injury with objectified neurological findings after fracture or developed due to other illnesses. • Pathologic fracture. • New fractures of ipsilateral or contralateral shoulders/arm that could influence the Active Range of Motion.

Design outcomes

Primary

MeasureTime frame
• Range of Motion (RoM)

Secondary

MeasureTime frame
• Length of the clavicle: on a conventional X-ray and measured with the 3D-Electromagnetic Motion Tracking Device. • DASH Outcome Measure

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)