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Buzzy for Chronic Pain
N/A
Waitlist Available
Led By Frederic Gerges, MD
Research Sponsored by Steward St. Elizabeth's Medical Center of Boston, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients receiving lidocaine infusions at the pain clinic.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 2 months
Awards & highlights
Study Summary
This trial is testing a device to reduce IV pain during lidocaine infusions for adults with chronic pain.
Eligible Conditions
- Chronic Pain
- Acute Pain
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an average of 2 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 2 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pain
Secondary outcome measures
Satisfaction on the Visual Analog Scale
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: BuzzyExperimental Treatment1 Intervention
Buzzy will be applied 5 to 10 cm proximal (toward the subject's head) to the dorsum of the hand site immediately prior and throughout the intravenous catheter insertion attempt.
Group II: No BuzzyActive Control1 Intervention
Subjects will have a 20g intravenous catheter inserted either in the left or right dorsum side of the hand without the Buzzy device.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Buzzy
2018
Completed Phase 2
~1240
Find a Location
Who is running the clinical trial?
Steward St. Elizabeth's Medical Center of Boston, Inc.Lead Sponsor
25 Previous Clinical Trials
5,741 Total Patients Enrolled
Frederic Gerges, MDPrincipal InvestigatorPain Medicine Physician
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Buzzy
- Group 2: No Buzzy
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is this study enlisting new participants at present?
"Indeed, research posted on clinicaltrials.gov points to an active recruitment period that began October 1st 2022 and was most recently updated December 14th 2022. This study is seeking 100 participants from a single site."
Answered by AI
What is the overall admission capacity for this clinical research?
"Yes, the information posted on clinicaltrials.gov implies that this trial is presently seeking participants. The original posting date was October 1st 2022 and it has recently been updated on December 14th of the same year. To complete recruitment, a total of 100 subjects need to be enrolled at one location."
Answered by AI
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