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Lidocaine for Pain
Phase 2 & 3
Waitlist Available
Led By Michael Norton, MD
Research Sponsored by Wake Forest University Health Sciences
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up following administration of a sub-induction dose of propofol, 0.5 mg/kg up to 50 mg, just prior to full induction
Awards & highlights
Study Summary
This trial tests whether esmolol and lidocaine can relieve propofol injection pain better than a placebo.
Eligible Conditions
- Pain
- Injection Site Reaction
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ following administration of a sub-induction dose of propofol, 0.5 mg/kg up to 50 mg, just prior to full induction
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~following administration of a sub-induction dose of propofol, 0.5 mg/kg up to 50 mg, just prior to full induction
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pain with propofol injection
Secondary outcome measures
Blood pressure
Heart rate
Oxygen saturation
Trial Design
3Treatment groups
Active Control
Placebo Group
Group I: LidocaineActive Control1 Intervention
1 mg/kg lidocaine to a max of 100 mg
Group II: EsmololActive Control1 Intervention
0.5 mg/kg esmolol to a max of 50 mg
Group III: PlaceboPlacebo Group1 Intervention
Saline water
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Who is running the clinical trial?
Wake Forest University Health SciencesLead Sponsor
1,250 Previous Clinical Trials
1,007,145 Total Patients Enrolled
22 Trials studying Pain
2,415 Patients Enrolled for Pain
Michael Norton, MDPrincipal InvestigatorWake Forest University Health Sciences
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have used opioids within the last three months.You are pregnant.You have a serious heart, lung, or liver problem.You cannot be intubated while awake and must be put to sleep with medication.You may have a blocked airway which could make breathing difficult.You are allergic to the medications being used in the study.You have not taken opioid pain medication, nonsteroidal anti-inflammatory drugs (NSAIDs), or other pain relievers within the last 24 hours.You have long-term pain and/or fibromyalgia.
Research Study Groups:
This trial has the following groups:- Group 1: Lidocaine
- Group 2: Esmolol
- Group 3: Placebo
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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