Mobile Monitoring of Fracture Healing

Tibial Fractures Clinical Trial

Official title:

Mobile Monitoring of Fracture Healing

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02534259
• Other study ID #: STUDY00002137
• Status: Completed
• Start date: August 2015
• Est. completion date: March 14, 2018

Study information

• Verified date: February 2019
• Source: Milton S. Hershey Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The objective of this study is to develop methods for using forces measured on circular external fixators to predict the state of individual patient's healing of severe tibial fractures and defects.

Description:

Patients receiving external fixators for tibial fractures and defects will be recruited. Normal struts on the device will be substituted with similar but instrumented struts which enable force measurement. During clinical visits, forces in the fixator, plus foot forces, will be measured during ambulation. Changes in force measurements across treatment and bone healing will be analyzed.

Severe fractures in the lower limb are associated with high energy trauma in both civilian and military patients,and are sometimes treated with external fixation devices to stabilize the bone until healing has occurred. The devices are kept on the patient for up to a year or more at significant cost, intrusiveness, and risk of infection. The clinician must decide when to remove the device such that adequate healing has occurred and the bone will not re-fracture, but healing rates are variable and x-rays can be misleading. The clinician must also identify when a patient is starting to progress poorly and an early revision surgery is needed to prevent further complications.

The investigators' goal is to develop novel approaches for instrumenting and collecting mechanical data from orthopaedic braces and devices, and identifying new methodologies for interpreting this large volume of functional data for optimizing personalized treatment. The present study is focused on external fixators. Strain gauges will be adhered to the fixators so that fixator forces can be measured during clinical visits. In this pilot study the investigators will develop methods to predict healing based on these measured forces.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 6
• Est. completion date: March 14, 2018
• Est. primary completion date: March 14, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. 18 to 80 years of age

2. Patients scheduled to undergo or currently undergoing treatment at Hershey Medical Center for tibia fracture and/or defect using a circular external fixator including Ilizarov and Taylor Spatial Frame types.

3. Ability to perform study procedures including ambulation (with assistance device if needed)

Exclusion Criteria:

1. External fixator design that cannot be suitably instrumented for force measurements due to space constraints or other issues

2. Axially stable fracture

3. Inability to understand English

4. Inability to provide informed consent

5. Difficulty maintaining follow-up

Related Conditions & MeSH terms

• Fractures, Bone
• Tibial Fractures

Intervention

Other:
• Force monitoring of external fixator struts

Locations

Country	Name	City	State
United States	Penn State Hershey Medical Center	Hershey	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Milton S. Hershey Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Radiographic and other clinical assessment of bone healing during clinical visits	Simultaneously measured during outcome 1 measurements	Approximately 5 times across treatment, with treatment lasting months to a year or more
Primary	Forces measured in the external fixator during ambulation during clinical visits		Approximately 5 times across treatment, with treatment lasting months to a year or more
Secondary	Forces measured in instrumented insoles during ambulation during clinical visits	Simultaneously measured during outcome 1 measurements	Approximately 5 times across treatment, with treatment lasting months to a year or more