Pediatric Locking Nail for the Treatment of Femoral Fractures in Children (PLN)
This study is ongoing, but not recruiting participants.
Sponsor:
Biomet, Inc.
Information provided by (Responsible Party):
Biomet, Inc.
ClinicalTrials.gov Identifier:
NCT00725894
First received: July 29, 2008
Last updated: November 6, 2012
Last verified: November 2012
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Purpose
The purpose of this multi-center prospective clinical outcomes study is to determine validity and safety of the pediatric locking nail for femoral fracture management in children with open physes.
| Condition | Intervention |
|---|---|
|
Femur Fracture |
Device: Pediatric Locking Nail |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | A Prospective Multi-Center Clinical Outcomes Study To Assess The Safety and Effectiveness Of The Pediatric Locking Nail For Treatment Of Femoral Fractures In Children |
Resource links provided by NLM:
Further study details as provided by Biomet, Inc.:
Primary Outcome Measures:
- limb alignment [ Time Frame: 48 months ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- length of healing, weight-bearing time (time to full weight bearing), and length of hospital stay and absence of complications [ Time Frame: 48 Months ] [ Designated as safety issue: Yes ]
| Enrollment: | 33 |
| Study Start Date: | November 2007 |
| Estimated Study Completion Date: | December 2013 |
| Estimated Primary Completion Date: | December 2013 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
1
The Pediatric Locking Nail was designed to provide stable sub-rigid fixation of femoral fractures in children
|
Device: Pediatric Locking Nail
The nail is pre contoured with a nine-degree anterior bow and is universal for right and left femoral.
|
Eligibility| Ages Eligible for Study: | 8 Years to 16 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Pediatric femoral fractures in patients 8-16 years of age where a nail is preferred
Criteria
Inclusion Criteria:
- Subject, representative willing to sign informed consent.
- Ability and willingness of the subject to follow postoperative care instructions until healing is complete
- Subject age must be between 8-16 inclusive.
- Subjects with a minimal canal diameter of 9mm or greater
And any of the following fracture types
- Non-comminuted and comminuted mid-shaft fractures
- Distal third fractures 4 cm above the distal physis
- Fractures that are open or closed
- Subtrochanteric fractures
Exclusion Criteria:
- A subject has a bone or soft tissue infection.
- Subject has a systemic infection.
- Subject has a distal (supracondylar) fracture.
- Subject with pathological bone (osteogenesis imperfecta and other conditions resulting in abnormal bone quality).
- Subjects with mental or neurological condition who are unwilling or incapable of following postoperative care instructions.
- Subject with conditions including blood supply limitation, and insufficient quantity or quality of bone.
- Foreign body sensitivity, where material sensitivity is suspected, testing is to be completed prior to implantation of device if at all practical or the subject should be excluded.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00725894
Locations
| United States, Arizona | |
| Phoenix Childrens Hospital | |
| Phoenix, Arizona, United States, 85016 | |
| United States, Florida | |
| Arnold Palmer Hospital for Children/OH Pediatric Orthopedics Clinic | |
| Orlando, Florida, United States, 32806 | |
| United States, North Carolina | |
| Orthopedic Clinical Research | |
| Charlotte, North Carolina, United States, 28204 | |
Sponsors and Collaborators
Biomet, Inc.
Investigators
| Study Chair: | Russell Schenck, PhD | Biomet, Inc. |
More Information
No publications provided
| Responsible Party: | Biomet, Inc. |
| ClinicalTrials.gov Identifier: | NCT00725894 History of Changes |
| Other Study ID Numbers: | CS-010 |
| Study First Received: | July 29, 2008 |
| Last Updated: | November 6, 2012 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Femoral Fractures Fractures, Bone Wounds and Injuries Leg Injuries |
ClinicalTrials.gov processed this record on May 19, 2013