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.
RECRUITING
800 participants
OBSERVATIONAL
2019-01-01
2026-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
It could be hypothesized that patients with proximal humeral fractures would benefit from this 3D classification, but there is a scarcity of application of the classification in large samples. T
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Analysis of Four-fragment Fractures of the Proximal Humerus: the Interest of 2D and 3D Imagery and Inter- and Intra-observer Reproducibility
NCT03646253
Detecting Occult Proximal Humeral Neck Fractures Through CT and MRI Tests of Patients With Greater Tuberosity Fractures
NCT03481478
Proximal Humerus Fractures: A Retrospective Analysis
NCT03637608
Operative Plate Fixation Versus Conservative Treatment for Acute, Displaced Fractures of Humeral Shaft
NCT03358173
Proximal Humerus Fracture Dislocation Direction and Avascular Necrosis
NCT05735561
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
patients wiht CT data
all patients with CT data are enrolled with this research, and the classification about proximal humeral fractures are identified.
without intervention, just retrospectively review the data about patients
without intervention
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
without intervention, just retrospectively review the data about patients
without intervention
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Clear record of demographic data;
* Three dimensional construction with mimics (with CT of B30);
* Patients older than 17 years with displaced PHF occurring less than 3 weeks before allocation and treatment.
Exclusion Criteria
* Open fractures;
* Pathological fracture (other than osteoporotic);
* Not a resident in the hospital catchment area
17 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hebei Medical University Third Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
the Third Hospital of Hebei Medical University
Shijiazhuang, Hebei, China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Chen Wei
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
JLGuo001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.