Ignite Creation Date:
2024-05-06 @ 10:03 AM
Last Modification Date:
2024-10-26 @ 12:23 PM
Study NCT ID:
NCT03145207
Status:
COMPLETED
Last Update Posted:
2020-07-09
First Post:
2017-05-03
Brief Title:
PK and DPK of Lidocaine Dermal Products
Sponsor:
University of Maryland Baltimore
Organization:
University of Maryland Baltimore
Study Overview
Official Title:
Evaluation of Bioavailability of Lidocaine Dermal Products
Status:
COMPLETED
Status Verified Date:
2020-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This is a bioequivalence study to compare lidocaine release between a brand name and generic skin patches in healthy adults
Detailed Description:
This research study is intended to determine the effect of heat on lidocaine patches This study will use lidocaine patches brand name and generic patches that have been approved by the Food and Drug Administration FDA and are already sold to customers in the United States and will not include any placebos
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None