Actively Recruiting
Management of Closed Diaphyseal Displaced Leg Fractures in Children and Adolescents
Led by University Hospital, Strasbourg, France · Updated on 2024-07-16
130
Participants Needed
1
Research Sites
38 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Most displaced tibial shaft fractures in pediatric patients have traditionally been treated after reduction by cast immobilization with good long-term results. Recently, there has been a growing trend towards surgical intervention by osteosynthesis from the outset. This study aims to describe the results of orthopedic treatment and osteosynthesis from the outset.
CONDITIONS
Official Title
Management of Closed Diaphyseal Displaced Leg Fractures in Children and Adolescents
Who Can Participate
Eligibility Criteria
You may qualify if you...
Inclusion Criteria:
- Minor subject (under 18 years old)
- Subject treated at the HUS, between June 1, 2004 and April 31, 2024, for a fracture of the displaced diaphysis of the tibia treated orthopedically or by osteosynthesis reviewed after more than 6 months
- Absence of written opposition in the medical file of the subject (and/or their legal representative if applicable) to the reuse of their data for scientific research purposes.
Exclusion criteria:
- Presence of opposition from the subject (and/or their legal representative if applicable) to the reuse of their data for scientific research purposes.
- Non-displaced and/or displaced fracture not located at the level of the tibial diaphysis
- Open fracture
- Incomplete or unusable file
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
Service de Chirurgie Pédiatrique - CHU de Strasbourg - France
Strasbourg, France, 67091
Actively Recruiting
Research Team
P
Philippe GICQUEL, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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