Viewing Study NCT01966263



Ignite Creation Date: 2024-05-06 @ 2:03 AM
Last Modification Date: 2024-10-26 @ 11:13 AM
Study NCT ID: NCT01966263
Status: COMPLETED
Last Update Posted: 2023-01-25
First Post: 2013-10-11

Brief Title: Fast Track Total Knee Arthroplasty Local Infiltration Analgesia vs Femoral Nerve Block
Sponsor: Sint Maartenskliniek
Organization: Sint Maartenskliniek

Study Overview

Official Title: Fast-track Rehabilitation Protocol for Total Knee Arthroplasty A Randomized Controlled Trial Comparing Local Infiltration Analgesia With Femoral Nerve Block
Status: COMPLETED
Status Verified Date: 2022-04
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: The objective of this study is to determine whether either a femoral nerve block FNB or local infiltration analgesia LIA is a better anesthetic technique to achieve optimal functional outcome after one year in patients receiving a total knee arthroplasty and following a fast track rehabilitation protocol
Detailed Description: For an optimal and fast recovery after total knee arthroplasty TKA a fast track rehabilitation protocol has been developed The literature is not yet conclusive about the optimal anesthestic technique The optimal technique should support fast mobilization by giving good pain relieve with minimal side effects such as nausea drowsiness and muscle weakness If pain relieve is optimal the patient mobilizes fast and length of stay is shortened But does fast recovery lead to better functional outcome The objective of this study is to determine whether either a femoral nerve block FNB or local infiltration analgesia LIA is a better anesthetic technique to achieve optimal functional outcome after one year in patients receiving a total knee arthroplasty and following a fast track rehabilitation protocol

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
Secondary IDs
Secondary ID Type Domain Link
2013-001008-13 EUDRACT_NUMBER None None
NL4396507213 OTHER CCMO register None