Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03625154
Other study ID # Pro47932
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2018
Est. completion date December 30, 2020

Study information

Verified date August 2018
Source Cedars-Sinai Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary objective of this study is to determine the failure rate and difference in clinical outcomes between operative and non operative treatment of patients with Weber B lateral malleolus ankle fractures with medial clear space widening on gravity stress views. All patients presenting will be treated non operatively, and compared to an observational group comprised of patients with Weber B lateral malleolus ankle fractures without medial clear space widening, for which the standard of care is non operative management.

Patients who decline non operative management and elect to undergo operative open reduction internal fixation with plates and screws will comprise an operative observational cohort.

All patients will be followed for a total of 12 months from the time of injury. Clinical outcomes will be based on radiographic monitoring for ankle mortise congruency, as well as standardized SF-36 and AOFAS questionnaire scores.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date December 30, 2020
Est. primary completion date July 18, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- 18-65 years old

- able to provide informed consent

Exclusion Criteria:

- pregnancy

- prisoners

- psychiatric conditions that prevent ability to provide informed consent or present barriers to follow up

- insulin dependent diabetics

- patients with prior musculoskeletal issues affecting the same extremity

- Patients cannot simultaneously be enrolled in any other studies.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ankle open reduction internal fixation
Open Reduction and Internal Fixation with plates and screws
Other:
non operative management
closed reduction and splinting followed by progressive weight bearing

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cedars-Sinai Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary radiographic outcome of ankle congruency measurement of medial clear space between medial malleolus and medial talar dome, measurement of tibiofibular overlap 1cm superior to the plafond, and measurement of superior clear space between the tibial plafond and the talar dome 1 year
Secondary functional outcome by American Orthopedic Foot and Ankle Score (AOFAS) scoring system total score 0-100, with 100 being the maximum best score. (pain (0-40 points), function (0-50 points) and alignment (0-10 points) 1 year
Secondary additional functional outcome by Short Form Survey (SF-36) Score scoring system 0 to 100 range, 100 being the best; subscores Physical functioning (0-10), Role limitations due to physical health (0-4), Role limitations due to emotional problems (0-3), Energy/fatigue (0-4)Emotional well-being (0-5), Social functioning (0-2), Pain (0-2), General Health 0-5 1 year
Secondary functional outcome by American Orthopedic Foot and Ankle Score (AOFAS) - Pain score none, mild occasional, moderate daily, severe and almost always present 1 year
Secondary functional outcome by American Orthopedic Foot and Ankle Score (AOFAS) - function - activity limitations, support requirements no limitations and no support, no limitation of daily activities but limitation of recreational activities, limited daily and recreational activities, or severe limitation of daily and recreational activities 1 year
Secondary functional outcome by American Orthopedic Foot and Ankle Score (AOFAS) - alignment good plantigrade, midfoot well aligned; fair plamtigrade, some degree of midfoot malalignment, poor with nonplantigrade foot, severe malalignment 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT05555459 - Performance and Safety Evaluation of Inion CompressOn Screw in Foot and Ankle Surgeries. PMCF Investigation N/A
Completed NCT04235907 - Telerehabilitation Following Ankle Fractures N/A
Completed NCT02949674 - Ropivacaine Versus Bupivacaine as Preemptive Analgesia in Surgical Site in Ankle Fracture Patients Phase 3
Completed NCT02198768 - Ankle Fracture vs Ankle Fracture-Dislocation
Recruiting NCT05916300 - Diagnostic Ultrasonography in Physiotherapy
Recruiting NCT04674046 - Deep Deltoid Ligament Integrity in Weber B Ankle Fractures - Mini-invasive Arthroscopic Evaluation. N/A
Recruiting NCT03696199 - Randomized Controlled Trial for Ankle Fracture Pain Control Phase 4
Recruiting NCT03259204 - Swedish Multicenter Trial of Outpatient Prevention of Leg Clots N/A
Active, not recruiting NCT03769909 - Prevention of Posttraumatic Osteoarthritis After Acute Intraarticular Fractures
Recruiting NCT05280639 - Simplified Post Op Rehabilitation for Ankle and Pilon Fractures N/A
Completed NCT02967172 - Efficacy of Multimodal Periarticular Injections in Operatively Treated Ankle Fractures Phase 4
Withdrawn NCT04768478 - CBD for Pain Reduction and Opioid Use After Ankle and Tibia Fracture ORIF Phase 4
Completed NCT05084794 - The Results of Middle-sized Posterior Malleolus Fractures: Fixed Versus Non-fixed N/A
Completed NCT03741556 - Prognostic Factors Following Ankle Fractures
Active, not recruiting NCT02481076 - Compression in Anklefracture Treatment, The CAT-study N/A
Recruiting NCT05729542 - Comparing Clinical Outcomes of Suture Button Versus Fibulink Fixation for Acute Ankle Syndesmosis Injuries N/A
Not yet recruiting NCT06086223 - Functional Outcomes Following Ankle Fracture Fixation With or Without Ankle Arthroscopy N/A
Recruiting NCT05389436 - Outpatient Versus Inpatient Surgery for Ankle Fractures N/A
Not yet recruiting NCT06329752 - Sciatic Nerve Block for Ankle and Leg Fracture Manipulation in the Emergency Department N/A
Recruiting NCT05391464 - Nerve Block for Pain Control After Fracture Surgery N/A