Ignite Creation Date:
2024-05-06 @ 3:29 PM
Last Modification Date:
2024-10-26 @ 1:50 PM
Study NCT ID:
NCT04647084
Status:
WITHDRAWN
Last Update Posted:
2023-08-18
First Post:
2020-11-17
Brief Title:
Pilot Trial Comparing Buzzy to Intradermal Lidocaine for Peripheral IV Cannulation in Adults
Sponsor:
Steward St Elizabeths Medical Center of Boston Inc
Organization:
Steward St Elizabeths Medical Center of Boston Inc
Study Overview
Official Title:
Pilot Randomized Control Trial Comparing the Effectiveness of Buzzy Versus Intradermal Lidocaine for Peripheral Intravenous Cannulation in Adults
Status:
WITHDRAWN
Status Verified Date:
2022-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
The investigators were unable to begin work on this study
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
IV placement is necessary for surgical procedures 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
Detailed Description:
Currently some medical providers administer the IV without any pain-relieving techniques Some medical providers inject a numbing medication underneath the skin prior to the IV placement This requires an additional needle stick Some medical providers place a device called Buzzy on a patients 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 the injection of numbing medication underneath the skin for IV placement in adults This device has been FDA approved for use
The investigators are conducting this study to compare the effectiveness of the Buzzy device with that of the injection of numbing medication underneath the skin for IV placement in adults This device has been FDA approved for use
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None