Pain Management in Children Undergoing Supracondylar Humerus Fracture Repair (NCT01812863) | Clinical Trial Compass
WithdrawnNot Applicable
Pain Management in Children Undergoing Supracondylar Humerus Fracture Repair
Stopped: Our anesthesiologist was no longer available to assist.
United States0Started 2012-07
Plain-language summary
The purpose of this study is to determine if US-guided supraclavicular anesthetic blocks reduce postoperative pain, use of rescue medication, and improve functional outcomes in children who underwent surgery for supracondylar humerus fractures.
Who can participate
Age range2 Years – 10 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients between 2 and 10 years old undergoing reduction and closed pinning of supracondylar humerus fractures
* Ability to obtain consent from the parents for participation in the study
* Patient has the ability to follow commands and train preoperatively the finger movements that are needed to determine nerve integrity.
* Written informed consent from the parent or guardian
Exclusion Criteria:
* Children with significant preoperative swelling in the elbow, as determined by the surgeon, that may lead to compartment syndrome
* Children with the potential for nerve entrapment as demonstrated by preoperative nerve deficit examination
* Children who have any contraindications (relative and absolute) to a supraclavicular block, including anticoagulation or coagulopathy, as well as patients that have active pulmonary disease that may exhibit respiratory compromise in response to potential phrenic nerve palsy or pneumothorax
What they're measuring
1
Rescue medication
Timeframe: In PACU following surgery
Trial details
NCT IDNCT01812863
SponsorAnn & Robert H Lurie Children's Hospital of Chicago