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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02736370
Other study ID # 2016-081
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2016
Est. completion date February 2019

Study information

Verified date September 2023
Source Spectrum Health Hospitals
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this observational study is to assess the rate of return to work, rate of return to activities, functional outcome measures and pain scores in operatively repaired rotational Bimalleolar and Trimalleolar (AO/OTA Classification of 44A and 44B) ankle fractures not requiring fixation of the syndesmosis and allowed early weight bearing on or before the first post-operative visit.


Recruitment information / eligibility

Status Completed
Enrollment 19
Est. completion date February 2019
Est. primary completion date February 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Men and women ages of 18 and up - Closed, low-energy Bimalleolar and Trimalleolar rotational ankle fractures - Orthopaedic Trauma Association (OTA) classification of 44A and 44B - English speaking - Able and willing to consent Exclusion Criteria: - Open fractures - OTA classification of 43 and 44C - Patients with diabetes mellitus - No other lower extremity injuries that would affect functional outcomes - Previous use of walking aides - Patients with paralysis or hemiplegia - Ankle fractures requiring syndesmotic repair - Ankle fractures requiring fixation of the posterior malleolar - Associated neurovascular injury - Problems maintaining follow up (homeless or not willing to return for follow up) - Pathological fractures - Prisoners - Patients not allowed to bear weight before the 6 week post-operative follow up visit

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Spectrum Health Hospitals

Outcome

Type Measure Description Time frame Safety issue
Primary Functional Outcome Scores During follow up visits functional outcomes scores will be assess using the Foot and Ankle Score and the PROMIS (Patient Reported Outcomes Measurement Information System) Mobility Measure questionnaires. These forms will be analyzed together to determine the patients functional outcomes. 12 months post operatively
Secondary Return to work During follow up visits the patients return to work status will be assessed. up to 12 months
Secondary Fracture Healing During follow up visits fractures healing will be assessed by physician review of x-rays. up to 12 months
Secondary Pain Scores Pain Scores and PROMIS Pain Intensity and Interference questionnaires will be assessed during follow up. These forms will be analyzed together to determine the patients overall pain. 12 months post operatively
Secondary Post operative complications Post operative complications will be assessed during follow up visits. up to 12 months