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Sulfur hexafluoride lipid-type A microspheres for Appendicitis
Phase 2
Waitlist Available
Led By Tolulope Oyetunji, MD
Research Sponsored by Children's Mercy Hospital Kansas City
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 60 days
Awards & highlights
Study Summary
This study is evaluating whether contrast ultrasound may help improve the diagnosis of appendicitis in children.
Eligible Conditions
- Appendicitis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 60 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~60 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of Children With an Accurate Diagnosis of Appendicitis.
Secondary outcome measures
Definitive Diagnosis
Number of Participants Who Required Additional CT Scan
Percentage of Negative Appendectomies
+2 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: ExperimentalExperimental Treatment1 Intervention
IV sulfur hexafluoride lipid-type A microspheres, 0.03 mL/kg, up to 2 doses per examination, total dose not to exceed 4.8 mL. Single examination per patient.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Sodium 1,2-Dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol)
FDA approved
Find a Location
Who is running the clinical trial?
Children's Mercy Hospital Kansas CityLead Sponsor
245 Previous Clinical Trials
935,762 Total Patients Enrolled
7 Trials studying Appendicitis
1,880 Patients Enrolled for Appendicitis
Tolulope Oyetunji, MDPrincipal InvestigatorChildren's Mercy Hospital Kansas City
Frequently Asked Questions
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