Viewing Study NCT00490594


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Study NCT ID: NCT00490594
Status: UNKNOWN
Last Update Posted: 2008-10-20
First Post: 2007-06-20
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: SeriACLâ„¢ Device Trial for Anterior Cruciate Ligament (ACL) Reconstruction
Sponsor: Serica Technologies, Inc.
Organization:

Study Overview

Official Title: A Multi-Center Open Study to Evaluate the SeriACLâ„¢ Device for Primary Anterior Cruciate Ligament Repair
Status: UNKNOWN
Status Verified Date: 2008-10
Last Known Status: ACTIVE_NOT_RECRUITING
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 SeriACL device was developed as an alternative to an autograft (i.e., tissue that is taken from a patient's own body) or an allograft (i.e., tissue that is taken from a cadaver) for ACL reconstruction. The SeriACL device is made of silk yarns, knit and processed with SeriCoatâ„¢ surface treatment which makes it easier to wet the material. The SeriACL device is designed to be a temporary support structure to replace the torn ACL and to stabilize the knee joint following surgical repair. It is designed to use the body's own healing process to regenerate the patient's own new ligament tissue. As the new tissue grows and the support structure is needed less over time, the SeriACL device is bioresorbed (i.e., broken down) by the patient's body. The SeriACL device is designed to be installed with standard surgical techniques for ACL repair.

This study is designed to test the safety of the SeriACL device in primary total ACL repair in patients with a torn ACL. The study will evaluate whether repair of the ACL with the SeriACL device will return the knee to normal function and what, if any, side effects will occur.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: