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Procedure

Fibular Nail vs. Standard Fixation for Ankle Fracture

N/A
Recruiting
Led By Kelly Hynes, MD
Research Sponsored by University of Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age 18 or older
Unstable ankle fracture
Must not have
Fractures that the treating surgeon indicates requires a posterior approach to achieve stability
Any previous ligament or fracture surgery on the index ankle
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year post-operatively
Awards & highlights

Summary

This trial compares two methods of fixing broken ankle bones in diabetic patients. One method uses a rod inside the bone to keep it stable, while the other is a more traditional surgery. The goal is to see which method leads to fewer complications and better recovery. Using a rod inside the bone may help reduce complications in patients with other health issues.

Who is the study for?
This trial is for diabetic adults over 18 with unstable ankle fractures and specific blood sugar levels (HbA1c > 6.5, fasting BG > 120, non-fasting BG > 200). It excludes those with open fractures, previous ankle surgeries, immune deficiencies like HIV or hepatitis, multiple injuries that affect mobility, active infections at the fracture site, or who can't follow the study protocol.
What is being tested?
The study compares two treatments for ankle fractures in diabetics: fibular intramedullary nail (IMFN) and standard open reduction and internal fixation (ORIF). The goal is to see if there's a difference in complication rates between these methods. This has not been studied before in diabetic patients.
What are the potential side effects?
Potential side effects may include complications related to surgery such as infection risk at the surgical site, pain around the area of operation, possible damage to nearby nerves or blood vessels during surgery, and general risks associated with anesthesia.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 18 years old or older.
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I have a recent, unstable fracture in my ankle.
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I have diabetes with high blood sugar or HbA1c levels.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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My surgeon recommends a specific surgery from the back to stabilize my fracture.
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I have had surgery on my ankle for a ligament issue or fracture.
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I have a broken bone that is exposed through my skin.
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I have multiple injuries on my limbs that affect my ability to move.
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I have an active infection or wound on my ankle.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year post-operatively
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year post-operatively for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Composite complication rate
Secondary study objectives
Patient reported outcome scores

Trial Design

2Treatment groups
Active Control
Group I: Fibular intramedullary nailActive Control1 Intervention
Randomized in the OR to ankle fracture repair with fibular intramedullary nail
Group II: Open reduction and internal fixation (ORIF)Active Control1 Intervention
Randomized in the OR to ankle fracture repair with ORIF

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for ankle fractures include fibular intramedullary fixation (IMFN) and open reduction and internal fixation (ORIF). IMFN stabilizes the fibula by inserting a rod into the medullary cavity, which supports bone healing and reduces complications, particularly in high-risk patients like diabetics. ORIF involves surgically exposing the fracture site to realign the bones and securing them with plates and screws. Both methods aim to stabilize the fracture, ensure proper alignment, and facilitate healing, but IMFN may offer advantages in terms of reduced surgical trauma and potentially lower complication rates. Understanding these mechanisms is crucial for patients to make informed decisions about their treatment options.

Find a Location

Who is running the clinical trial?

University of ChicagoLead Sponsor
1,034 Previous Clinical Trials
753,574 Total Patients Enrolled
Kelly Hynes, MDPrincipal InvestigatorUniversity of Chicago

Media Library

Fibular intramedullary nail (Procedure) Clinical Trial Eligibility Overview. Trial Name: NCT05204485 — N/A
Ankle Fracture Research Study Groups: Fibular intramedullary nail, Open reduction and internal fixation (ORIF)
Ankle Fracture Clinical Trial 2023: Fibular intramedullary nail Highlights & Side Effects. Trial Name: NCT05204485 — N/A
Fibular intramedullary nail (Procedure) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05204485 — N/A
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