Ignite Creation Date:
2024-05-05 @ 12:03 PM
Last Modification Date:
2024-10-26 @ 9:19 AM
Study NCT ID:
NCT00226772
Status:
COMPLETED
Last Update Posted:
2012-10-12
First Post:
2005-09-26
Brief Title:
Efficacy and Safety of OMS103HP in Patients Undergoing Autograft Anterior Cruciate Ligament ACL Reconstruction
Sponsor:
Omeros Corporation
Organization:
Omeros Corporation
Study Overview
Official Title:
Double-Blind Multicenter Phase 3 Study Comparing the Efficacy and Safety of OMS103HP With Vehicle in Patients Undergoing Autograft ACL Reconstruction
Status:
COMPLETED
Status Verified Date:
2012-10
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 anterior cruciate ligament ACL is an important stabilizer of the knee Orthopedic surgeons replace the torn ligament during ACL reconstruction surgery Surgical trauma initiates an acute inflammatory response including swelling and pain that leads to restricted joint motion and loss of function OMS103HP was designed to deliver targeted therapeutic agents directly to the surgical site during the arthroscopic procedure to inhibit inflammation and pain before they can begin
The purpose of this study is to assess the effectiveness and safety of OMS103HP in improving knee function following ACL reconstruction using a hamstring autograft Secondary benefits being evaluated include reduced postoperative pain improvement in knee range of motion and earlier return to work
The purpose of this study is to assess the effectiveness and safety of OMS103HP in improving knee function following ACL reconstruction using a hamstring autograft Secondary benefits being evaluated include reduced postoperative pain improvement in knee range of motion and earlier return to work
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