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Pin for Midshaft Clavicle Fractures
N/A
Waitlist Available
Led By Kyle J Jeray, MD
Research Sponsored by Prisma Health-Upstate
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
Study Summary
This trial will compare surgical and non-surgical treatment options for people with broken collar bones.
Eligible Conditions
- Midshaft Clavicle Fractures
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Disability of Arm, Shoulder and Hand (DASH) scores
Secondary outcome measures
Reoperation rate
Trial Design
3Treatment groups
Active Control
Group I: PinActive Control1 Intervention
Pin Fixation
Group II: ORIFActive Control1 Intervention
Open Reduction and Internal Fixation (ORIF) with Plate and Screws
Group III: ClosedActive Control1 Intervention
Closed Treatment
Find a Location
Who is running the clinical trial?
Prisma Health-UpstateLead Sponsor
82 Previous Clinical Trials
42,526 Total Patients Enrolled
Orthopaedic Trauma AssociationOTHER
32 Previous Clinical Trials
4,604 Total Patients Enrolled
Indiana UniversityOTHER
980 Previous Clinical Trials
982,749 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have a broken bone where your collarbone meets your breastbone.You have a bone fracture where the bone is exposed through the skin.You have a broken collarbone in the middle part.You have a broken collarbone that is displaced or shortened by 1.5 cm or more.You have an injury in the ligaments on the side of your body.You have a broken bone that is affecting your nerves or blood vessels.You have a broken bone that is causing damage to the skin around it.You have injuries to the same side of your upper body as your shoulder.
Research Study Groups:
This trial has the following groups:- Group 1: Pin
- Group 2: ORIF
- Group 3: Closed
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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