Viewing Study NCT00338663



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Last Modification Date: 2024-10-26 @ 9:25 AM
Study NCT ID: NCT00338663
Status: COMPLETED
Last Update Posted: 2007-08-23
First Post: 2006-06-16

Brief Title: A Study on Knee Immobilization and Pain Levels After an Anterior Cruciate Ligament ACL Reconstruction Surgery
Sponsor: LifeMark Health Research Group
Organization: LifeMark Health Research Group

Study Overview

Official Title: The Effect of Knee Immobilization on Postoperative Pain Following an Anterior Cruciate Ligament ACL Reconstruction A Randomized Clinical Trial
Status: COMPLETED
Status Verified Date: 2007-08
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 purpose of the study is to determine if there is difference in immediate postoperative pain levels 48 hours between patients who wear a knee immobilizer splint compared to patients who do not wear a knee immobilizer splint after an anterior cruciate ligament reconstruction surgery
Detailed Description: This study will attempt to evaluate the efficacy of knee immobilization on patient postoperative pain levels following an ACL reconstruction There is a lack of consensus in the area of postoperative knee bracingimmobilization A survey of Canadian surgeons indicates that the primary reason for postoperative knee immobilization is to reduce pain To the investigators knowledge there are no studies comparing the use of immediate 0-48 hours postoperative knee immobilization versus no immobilization and pain control in this patient population

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