Evaluation of Handling and Possible Complications Related to the Newly Developed Angular Stable Locking System (ASLS) (ASLS-Pre)

AO Clinical Investigation and Publishing Documentation

Status: Completed

Conditions: Humerus Fracture; Tibia Fracture; Femur Fracture

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT00793637

ASLS-Pre-08

Details and patient eligibility

About

In many cases, the existing locking bolts and screws in intramedullary nails do not provide sufficient stability. Due to the play between screw and nail, the reduction can be lost and the instability can result in malunions, nonunions, or pseudoarthrosis. Consequently, secondary angular fracture dislocation (defined as a difference of the angle of 10° or more from the post-operative to the follow-up x-rays) can be observed in approximately 30% of patients after conventional intramedullary nailing of proximal third tibial fractures and in approximately 0-2% in patients with distal third tibial fractures. Therefore, an Angular Stable Locking System for Intramedullary Nails (ASLS) was developed to reduce the risk of secondary loss of reduction by providing axial and angular stability. ASLS provides angular stable fixation between nails and screws with resorbable sleeves used as dowels in the nail locking holes.

The present study evaluates the handling of ASLS and the surgeon's compliance as well as any complications occurring during the baseline and the follow-up period in patients with proximal and distal tibial, femoral and humeral fractures treated with intramedullary nails. Furthermore, the relationship of any occurred complications to ASLS will be assessed.

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• The patient is ≥ 18 years old
• One of the following bones is fractured so that the fracture is affecting the proximal or the distal third of the bone without affecting the joint surface: Humerus, Femur, Tibia
• The fracture is fixed with one of the following cannulated implants Humerus: Expert HN, Expert PHN. Femur: Expert LFN, Expert RAFN, CFN, DFN, AFN. Tibia: Expert TN, CTN.
• The patient is willing and able to participate in the study follow-up according to the CIP.
• The patient is able to understand and read local language at elementary level.
• The patient is willing and able to give written informed consent to participate in the study.

Exclusion criteria

• The patient is legally incompetent.
• Preexistent malunion or nonunion of the bone that is planned to be treated with ASLS.
• The patient suffers from a polytrauma (multiple injuries, whereof one or the combination of several injuries is life-threatening).
• The patient suffers from active malignancy.
• The patient is affected by drug or alcohol abuse.
• The patient has participated in any other device or drug related clinical trial within the previous month.

Trial design

30 participants in 1 patient group

Surgical

Description:

Patients with proximal and/or distal tibial, femoral and/or humeral fractures treated with intramedullary nails and the Angular Stable Locking System(ASLS)