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Local Anesthetic
Arm A for Local Anesthesia
Phase 4
Waitlist Available
Led By Joseph McBride, MD
Research Sponsored by University of Nebraska
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
adults presenting for routine thyroid biopsy, paracentesis or thoracentesis in interventional radiology
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
Study Summary
The purpose of this study is to determine the optimal amount of lidocaine buffering needed to decrease injection pain when administering local anesthesia.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Injection pain
Trial Design
4Treatment groups
Active Control
Group I: Arm AActive Control1 Intervention
10 mg/mL lidocaine; Frequency: 1
Group II: Arm BActive Control2 Interventions
9 mg/mL of 10% sodium bicarbonate-90% lidocaine; Frequency: 1
Group III: Arm CActive Control2 Interventions
7.5 mg/Ml of 25% sodium bicarbonate-75% lidocaine Frequency: 1
Group IV: Arm DActive Control2 Interventions
5 mg/mL 50% sodium bicarbonate-50% lidocaine Frequency: 1
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Who is running the clinical trial?
University of NebraskaLead Sponsor
537 Previous Clinical Trials
1,143,884 Total Patients Enrolled
Joseph McBride, MDPrincipal InvestigatorUniversity of Nebraska
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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