Long Term Follow up in Pediatric Supracondylar Humeral Fracture
NCT ID: NCT05780398
Last Updated: 2023-03-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
634 participants
OBSERVATIONAL
2023-03-31
2024-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The main questions it aims to answer are:
* how good is the elbow function
* what are the post-operative complication
* what is the time before return to sport
* what is the aesthetic prejudice of the scar for the patient Participants will answer questionnaries and send photographs of their elbows to the examinator
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Type II Pediatric Supracondylar Humerus Fracture Management and Outcomes: A Prospective Multi-centre Cohort Study
NCT02963233
Role of US vs X Ray in Detection of Pediatric Elbow Fractures.
NCT05968092
Non-operative Treatment of Pediatric Lateral Humeral Condyle Fractures
NCT05096689
Trial of Ultrasound Guidance for Reduction of Pediatric Forearm Fractures
NCT03097757
Pediatric Supracondylar Humerus Fracture NIRS Study
NCT01808183
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
As distal humerus is responsible for only 20% of humeral growth, bone remodelage her is less important compared to other sites in children..
Many different attitudes are possible : orthopedic reduction, open reduction, percutaneous pinning ... No methode as clearly demontrated a superiority.
Percutaneous pinning as been widely used the last years though We haven't find any study evaluating long term outcomes regarding functionnal and aesthetic outcomes in supracondylar humeral fracture treated by percutaneous pinning.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
RETROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Children who did not effectively suffered a supracondylar humeral fracture
1 Day
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Grenoble
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
38RC22.0384
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.