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Dual vs. Single Plate Fixation for Collarbone Fractures (COMPACT Trial)
N/A
Recruiting
Led By Ujash Sheth, MD MSc FRCSC
Research Sponsored by Sunnybrook Health Sciences Centre
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Between 18 and 65 years of age
A completely displaced midshaft fracture of the clavicle (no cortical contact between the main proximal and distal fragments (AO/OTA 15.2A/B/C))
Must not have
Significant medical comorbidities (i.e., ASA grade IV and V)
Concomitant ipsilateral upper extremity fracture
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average 2 years
Awards & highlights
No Placebo-Only Group
Summary
This trial compares two surgical methods for fixing broken collarbones in patients with acute displaced fractures. One method uses two smaller plates to reduce irritation, while the other uses a single larger, shaped plate. The goal is to see if the dual plating method results in fewer additional surgeries.
Who is the study for?
This trial is for adults aged 18-65 with a completely displaced midshaft fracture of the clavicle that can be fixed with plates and screws. Candidates must have had the injury within the last 28 days, be able to follow up, and give consent. Those with neurovascular injuries, significant other medical issues, open fractures or additional serious injuries are excluded.
What is being tested?
The study compares two surgical methods for fixing broken collarbones: one using dual mini-fragment plating and another using single precontoured plating. The goal is to see if dual plating leads to fewer repeat surgeries while maintaining similar healing rates and complications.
What are the potential side effects?
Potential side effects may include irritation at the site of implantation leading to possible removal of plates, infection risks from surgery, pain at the fracture site post-operation, and general risks associated with surgical procedures.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 18 and 65 years old.
Select...
I have a fully broken collarbone with no touching bone ends.
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My fracture can be fixed with a plate and at least three screws on each end.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have severe health problems besides my cancer.
Select...
I have a fracture in the same arm as my breast cancer.
Select...
I have had a fracture due to a disease.
Select...
I have a severe head injury.
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I have a broken bone that is exposed through my skin.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an average 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average 2 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Removal of hardware at two years of follow-up
Secondary study objectives
Adverse events/complications
Functional outcome ASES
Functional outcome DASH
+8 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Dual mini-fragment platingExperimental Treatment1 Intervention
Group II: Single precontoured platingActive Control1 Intervention
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 collarbone fractures, such as dual mini-fragment plating and single precontoured plating, work by mechanically stabilizing the fracture site to promote proper bone healing. Dual mini-fragment plating uses two smaller plates to distribute the mechanical load more evenly, which can reduce irritation and the need for reoperation compared to a single larger plate.
This method aims to maintain the alignment of bone fragments while minimizing soft tissue disruption. Intramedullary nailing, another common treatment, involves inserting a rod into the bone marrow cavity to stabilize the fracture from within, offering a minimally invasive option with good cosmetic and functional outcomes.
These treatments are crucial for patients as they directly impact the healing process, potential complications, and overall recovery experience.
Miniplate osteosynthesis in fracture surgeries: Case series with review of concepts.Plate Versus Intramedullary Fixation Care of Displaced Midshaft Clavicular Fractures: A Meta-Analysis of Prospective Randomized Controlled Trials.Surgical interventions for treating acute fractures or non-union of the middle third of the clavicle.
Miniplate osteosynthesis in fracture surgeries: Case series with review of concepts.Plate Versus Intramedullary Fixation Care of Displaced Midshaft Clavicular Fractures: A Meta-Analysis of Prospective Randomized Controlled Trials.Surgical interventions for treating acute fractures or non-union of the middle third of the clavicle.
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Who is running the clinical trial?
Canadian Orthopaedic Trauma SocietyOTHER
4 Previous Clinical Trials
380 Total Patients Enrolled
Sunnybrook Health Sciences CentreLead Sponsor
674 Previous Clinical Trials
1,565,789 Total Patients Enrolled
Ujash Sheth, MD MSc FRCSCPrincipal InvestigatorSunnybrook Health Sciences Centre
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am between 18 and 65 years old.I have a fully broken collarbone with no touching bone ends.I have severe health problems besides my cancer.I have a fracture in the same arm as my breast cancer.I have had a fracture due to a disease.I have a severe head injury.My fracture can be fixed with a plate and at least three screws on each end.I have a broken bone that is exposed through my skin.
Research Study Groups:
This trial has the following groups:- Group 1: Single precontoured plating
- Group 2: Dual mini-fragment plating
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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