Fracture Clinical Trial
Official title:
Phase 1 Study of Circadian Rhythm of Salivary Cortisol in Health Children ;Phase 2 Study of Circadian Rhythm of Salivary Cortisol of Children Undergoing Surgery Using Etomidate or Not Using Etomidate.
Etomidate is an unique drug used for induction of general anesthesia and sedation. Adrenal cortical inhibition by etomidate has received much attention. However wether the circadian rhythm and pulse secretion pattern of cortisol in children are the same as that in adults is not known. Moreover, the effect of etomidate on circadian rhythm changes and clinical outcomes has never been carefully studied in children undergoing surgery. Our hypothesis is that etomidate can relieve the changes of circadian rhythm of salivary cortisol in children for 24-48 hours,and this does not make clinical outcomes worse postoperatively.
- Sample size assessment: Using formula to calculate the total number is 30.
- Statistical analysis: ANOVA
- Reporting for adverse events: During the period of study, if there is any severe adverse
event happening, such as severe infection, severe low cortisol concentration threatening
the patient's life we will stop the trial.
;
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Withdrawn |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
|
||
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 | |
Completed |
NCT02786498 -
Optimal Vitamin D3 Supplementation Strategies for Acute Fracture Healing
|
Phase 2 |