Ignite Creation Date:
2024-05-06 @ 1:58 AM
Last Modification Date:
2024-10-26 @ 11:12 AM
Study NCT ID:
NCT01939379
Status:
WITHDRAWN
Last Update Posted:
2021-04-20
First Post:
2013-09-03
Brief Title:
Adductor Canal Nerve Block Following Total Knee Arthroplasty
Sponsor:
Loma Linda University
Organization:
Loma Linda University
Study Overview
Official Title:
Adductor Canal Nerve Block Following Total Knee Arthroplasty A Randomized Prospective Study Comparing High vs Low Volume Bolus of 033 Ropivacaine
Status:
WITHDRAWN
Status Verified Date:
2021-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
PI left institution Efforts made to contact PI unsuccessful No study data available
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is that an adductor canal nerve block putting numbing medicine near the nerve has been shown to produce excellent pain relief with less pain medication use after knee replacement surgeryThe investigators will be comparing the amount of pain relief following knee replacement surgery when you have a nerve block in place There will be approximately 66 subjects participating in this study After surgery subjects will receive numbing medication every 6 hours for 48 hours Subjects will also receive a morphine PCA patient controlled analgesia after surgery and pain medication by mouth every 4 hours around the clock with the option to receive more pain medication if needed Subjects will participate in the study up to 3 days
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None