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IVs With Buzzy in Chronic Pain Patients

IVs With Buzzy in Chronic Pain Patients

Status
Withdrawn
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05555173
Enrollment
0
Registered
2022-09-26
Start date
2022-10-01
Completion date
2023-10-20
Last updated
2026-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain, Acute Pain

Brief summary

The investigators are conducting a study to compare the effectiveness of the Buzzy® device with that of no pain relief method for IV placement in adults with chronic pain receiving lidocaine infusions.

Detailed description

IV placement is necessary for lidocaine infusions. Unfortunately, some patients say that placing an IV is painful. The investigators are conducting this study to evaluate two techniques that could make the placement of the IV more comfortable. Currently, some medical providers administer the IV without any pain-relieving techniques. Some medical providers place a device called Buzzy® on a patient's arm prior to the IV placement. The Buzzy® device is the combination of an ice pack and a vibrator in the shape of a bumble bee. Literature shows that the Buzzy® device makes IV placement more comfortable for children, but there is minimal data in regard to whether it is helpful for adult patients. The investigators are conducting this study to compare the effectiveness of the Buzzy® device with that of no pain relief method for IV placement in adults with chronic pain receiving lidocaine infusions. The use of the Buzzy® device in adults is the investigational part of the study. This device has been FDA approved for use.

Interventions

DEVICEBuzzy

Buzzy is a small vibrating bee with ice-pack wings.

Sponsors

Steward St. Elizabeth's Medical Center of Boston, Inc.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients receiving lidocaine infusions at the pain clinic.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Pain on the Numeric Rating Scalethrough study completion, an average of 2 monthsPatients are asked to report their subjective pain on the Numeric Rating Scale from 0 to 10, where 0 = No Pain and 10 = Worst Pain.

Secondary

MeasureTime frameDescription
Satisfaction on the Visual Analog Scalethrough study completion, an average of 2 monthsPatients are asked to report their subjective satisfaction with the IV placement on the Visual Analog Scale, where labeled face images represent satisfaction from very poor satisfaction to excellent satisfaction.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORFrederic Gerges, MD

Pain Medicine Physician

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026