Ankle Fracture vs Ankle Fracture-Dislocation

Ankle Fractures Clinical Trial

Official title:

Functional Outcome After Ankle Fractures and Ankle Fracture-Dislocations: A Prospective Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02198768
• Other study ID #: 06-12-03A
• Status: Completed
• Start date: September 2012
• Est. completion date: January 2017

Study information

• Verified date: January 2017
• Source: Wake Forest University Health Sciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of this study is to compare outcomes of patients with an ankle fracture to those with ankle fracture-dislocations. We hypothesize that long-term clinical outcomes for patients sustaining ankle fracture dislocations are poorer than those without dislocation.

Description:

Orthopaedic literature has very limited data regarding outcomes following ankle fracture dislocations. Increased knowledge of the long-term consequences of these injuries could usher in changes to treatment paradigms, potentially resulting in improved outcomes. Thirty patients will be enrolled into two arms of this prospective study: isolated ankle fractures and ankle fracture dislocations. Patients will be followed through their operative and postoperative course and clinical and radiographic assessments will be analyzed. We plan to compare the clinical, radiographic, and functional outcomes of patients with ankle fractures to those with ankle fracture-dislocations. We also plan to identify factors that contribute to or predict poor clinical, functional, and/or radiographic outcomes in patients with ankle fractures and fracture-dislocations.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: January 2017
• Est. primary completion date: November 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients who sustain an isolated bi-malleolar or trimalleolar ankle fracture or an ankle fracture-dislocation requiring open reduction internal fixation
• Patients ages 18 and over
• The subject is psychosocially, mentally, and physically able to understand and comply with the requirements of the study
• Open and closed fractures (excluding Gustilo grade 3)
• English must be patient's primary language

Exclusion Criteria:

• Previous injury or significant osteoarthritis to the affected ankle
• Current ipsilateral or contralateral lower extremity injury with the exception of a contralateral ankle fracture or fracture-dislocation
• Retained hardware from a previous injury at or around the tibia-talar joint of the affected extremity
• Patients under the age of 18
• History of inflammatory arthropathy
• Traumatic Brain Injury or Spinal Cord Injury preventing weightbearing on the lower extremities
• The subject has another concurrent physical or mental condition that is likely to affect compliance with the study requirements
• Patients with Gustilo grade 3B and 3C open fractures

Related Conditions & MeSH terms

• Ankle Fractures
• Fracture Dislocation
• Fractures, Bone

Locations

Country	Name	City	State
United States	Carolinas Medical Center- Main	Charlotte	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
Wake Forest University Health Sciences

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Additional surgical procedures	Documentation of any additional surgical procedures conducted on the affected ankle. Any surgical procedure will be noted. These may include debridement for infection or dehiscence, revision for hardware failure, arthroscopy, ankle arthrodesis, or cartilage restoration procedures.	2 years
Other	Postoperative Complications	Postoperative complications will be documented and analyzed to determine if there are significant differences between the two groups. These will include infection requiring antibiotics or debridement, hardware failure, nerve or vascular injury, deep venous thrombosis, or revision surgery.	2 years
Primary	Change in Functional Outcome	Clinical and functional outcomes will be measured using the Foot and Ankle Ability Measure (FAAM) and the Short Form Musculoskeletal Functional Assessment (SMFA).; Radiographic analysis will be performed to determine nonunion, malunion, joint space incongruity, hardware failure/loosening, and/or severity of osteoarthritis. The Van Dijk grading scale will be used for radiographic assessment.	6, 12, and 24 months
Secondary	Radiographic Outcome	Radiographic analysis will be performed to determine nonunion, malunion, joint space incongruity, hardware failure/loosening, and/or severity of osteoarthritis. The Van Dijk grading scale will be used for radiographic assessment.	24 month