Fracture Clinical Trial
Pain is a common cause for children seeking care in the Emergency Department (ED). Children
with orthopedic injuries often require pain control when seeking emergency care. Despite the
high prevalence of ED visits requiring pain control, pain is often poorly assessed and
treated in ED settings. Currently, no standard of care exists for the management of this
fracture-related pain in children discharged from the ED. Furthermore, discrepancies in
analgesia administration to patients of various racial groups seeking emergency care have
been documented but are poorly understood. No research currently exists comparing pain
severity between upper extremity fractures requiring simple splinting to those treated with
sedated reduction and splinting. Furthermore, there is no research regarding the prevalence
of significant post-discharge pain nor the differences among ethnic and age groups treated
in the ED.
Research Questions:
What is the prevalence of significant post-discharge pain in children treated for upper
extremity fractures?
Is there a difference in severity between those children requiring reduction versus simple
splinting?
Is there a difference in pain severity noted among different ethnic or age groups?
Design This is a prospective, un-blinded, observational study that will include patients
seeking treatment for an upper extremity fracture.
n/a
Observational Model: Case-Only, Time Perspective: Prospective
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT04470895 -
Impact of Drugs on the Risk of Falls in the Fracture Department of the Paris Saint-Joseph Hospital Group
|
||
Recruiting |
NCT02635022 -
Fragility Fracture Liaison Service and Anti-osteoporosis Medication Monitoring Service Study
|
||
Unknown status |
NCT02013986 -
Effects of Etomidate on Postoperative Circadian Rhythm Changes of Salivary Cortisol in Children
|
Phase 4 | |
Terminated |
NCT01248182 -
Bone to Skin Thickness Study: Obese Versus Normal Population
|
N/A | |
Recruiting |
NCT00969839 -
NovaLign Intramedullary Fixation System (IFS) for the Treatment of Humeral Fractures
|
Phase 4 | |
Completed |
NCT00115180 -
Racial and Ethnic Disparities in Acute Pain Control
|
N/A | |
Completed |
NCT00520442 -
Acute Pediatric Fracture Analgesia Study
|
N/A | |
Not yet recruiting |
NCT06402292 -
Surgical Treatment of Osteoarticular Infections Using Bioactive Bone Substitute
|
N/A | |
Recruiting |
NCT04947722 -
The PREVENT Trial: a Pragmatic Cluster Randomized Controlled Trial of a Multifaceted Fracture Prevention Model for Long-term Care
|
N/A | |
Recruiting |
NCT06107699 -
The CHARM Study-Coordinating Transitions From Hospital for Older Adults With Fractures
|
N/A | |
Completed |
NCT04532580 -
Clinical Validation of Boneview for FDA Submission
|
||
Completed |
NCT04237454 -
Thermal Imaging Compared to Skeletal Survey in Children Below 2 Years
|
N/A | |
Recruiting |
NCT05002335 -
Clinical and Radiological Outcomes of Medacta Shoulder System (BE)
|
||
Completed |
NCT02591043 -
Surgical Treatment of Low Energy Pelvic Fractures in the Elderly
|
N/A | |
Completed |
NCT02933359 -
Osteogenic Profiling of Normal Calvarial Bone
|
||
Completed |
NCT01049191 -
Bone Microarchitecture in Women With and Without Fracture
|
N/A | |
Completed |
NCT03431857 -
Multi Centre Study on TESS V2 Shoulder System
|
||
Recruiting |
NCT04133103 -
Early Mobilisation in the Surgical Robot Assisted Spinal Surgery
|
N/A | |
Completed |
NCT03993691 -
Wrist Fracture Evaluation With a Desktop Orthopedic Tomosynthesis System
|
N/A | |
Active, not recruiting |
NCT01719887 -
Effectiveness and Cost-effectiveness of Surgical Treatment of Humeral Shaft Fractures. Randomized Controlled Trial
|
N/A |