Humeral Compression/Distraction Device
Primary Purpose
Humeral Fractures
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Humeral Compression/Distraction (CD) Nail
Sponsored by
About this trial
This is an interventional treatment trial for Humeral Fractures focused on measuring upper extremity fracture
Eligibility Criteria
Inclusion Criteria:
Adult skeletally mature patients 18 years or older, treated by the Orthopaedic Trauma Service at Tampa General Hospital, and the Trauma Service at St. Louis University Hospital
- Open or closed displaced humeral shaft fractures (displaced OTA code 12A, B, or C), nonunions or malunions
- amenable to treatment with an intramedullary nail
Exclusion Criteria:
- Intra-articular extension of the fracture, prohibiting treatment with an intramedullary nail;
- Pathologic fracture
- Retained hardware
- Patients with pacemakers
- Age under 18 years.
- Patients who are prisoners or likely to become prisoners
- Homeless, or those likely to have difficulty making follow-up appointments
- Pregnancy
- Ipsilateral nerve or vascular injuries
- Immunocompromised patients
Sites / Locations
- Tampa General Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
humeral nail
Arm Description
Surgical fixation with a humeral compression/distraction nail.
Outcomes
Primary Outcome Measures
Union rate
Union rate for compression/distraction nail will be compared to retrospective cohort of surgical fixation with humeral plates.
Secondary Outcome Measures
Complication rate
Complication rate for compression/distraction nail will be compared to retrospective cohort of surgical fixation with humeral plates.
Adverse Events
Adverse event rate for compression/distraction nail will be compared to retrospective cohort of surgical fixation with humeral plates.
Full Information
NCT ID
NCT02861495
First Posted
August 3, 2016
Last Updated
September 5, 2018
Sponsor
Florida Orthopaedic Institute
Collaborators
NuVasive, St. Louis University
1. Study Identification
Unique Protocol Identification Number
NCT02861495
Brief Title
Humeral Compression/Distraction Device
Official Title
Humeral Compression/Distraction (CD) Device Used for Fixation of Humeral Fractures
Study Type
Interventional
2. Study Status
Record Verification Date
September 2018
Overall Recruitment Status
Terminated
Why Stopped
Study stopped due to low enrollment.
Study Start Date
September 30, 2016 (Actual)
Primary Completion Date
August 9, 2018 (Actual)
Study Completion Date
August 15, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Florida Orthopaedic Institute
Collaborators
NuVasive, St. Louis University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The proposed study of humeral shaft fractures in adults will examine outcomes in patients treated with the Humeral Trauma Nail System to treat displaced humeral shaft fractures (displaced OTA code 12A, B, or C), nonunions, or malunions. The device to be studied uses an internal gear system controlled wirelessly by rare earth magnets, which typically offers distraction for lengthening. In the humerus however, during the treatment of acute fractures, this percutaneously inserted nail can also offer compression during the healing process, thereby negating the effect of gravity, which may in turn lead to a faster and more consistent rate of union. Furthermore, in cases of slower healing the dynamic properties of the nail may employ an "accordion technique" (alternating compression-distraction, a feature unique to this implant.
Detailed Description
The primary end point will be the union rate without secondary procedures. The hypothesis is that with the compression and distraction that this device makes possible, the investigators can achieve a higher union rate than with other forms of treatment, using a percutaneous approach, with a decreased complication rate, and can dynamically modulate the healing response when needed. The primary safety endpoint is the occurrence of adverse events from the time of treatment.
During the healing process an external remote controller (ERC) will be used to continually compress or distract the fracture as needed. The surgeon will monitor healing and decide, clinically based on sequential radiographs during subsequent office visits, whether the fracture needs additional compression or distraction, an accordion technique, or no additional external manipulation via the ERC. Participants will be followed for 12 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Humeral Fractures
Keywords
upper extremity fracture
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)
8. Arms, Groups, and Interventions
Arm Title
humeral nail
Arm Type
Experimental
Arm Description
Surgical fixation with a humeral compression/distraction nail.
Intervention Type
Device
Intervention Name(s)
Humeral Compression/Distraction (CD) Nail
Intervention Description
Surgical fixation of humeral shaft fractures with Humeral Compression/Distraction (CD) Nail implant
Primary Outcome Measure Information:
Title
Union rate
Description
Union rate for compression/distraction nail will be compared to retrospective cohort of surgical fixation with humeral plates.
Time Frame
3 months post operatively
Secondary Outcome Measure Information:
Title
Complication rate
Description
Complication rate for compression/distraction nail will be compared to retrospective cohort of surgical fixation with humeral plates.
Time Frame
12 months
Title
Adverse Events
Description
Adverse event rate for compression/distraction nail will be compared to retrospective cohort of surgical fixation with humeral plates.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult skeletally mature patients 18 years or older, treated by the Orthopaedic Trauma Service at Tampa General Hospital, and the Trauma Service at St. Louis University Hospital
Open or closed displaced humeral shaft fractures (displaced OTA code 12A, B, or C), nonunions or malunions
amenable to treatment with an intramedullary nail
Exclusion Criteria:
Intra-articular extension of the fracture, prohibiting treatment with an intramedullary nail;
Pathologic fracture
Retained hardware
Patients with pacemakers
Age under 18 years.
Patients who are prisoners or likely to become prisoners
Homeless, or those likely to have difficulty making follow-up appointments
Pregnancy
Ipsilateral nerve or vascular injuries
Immunocompromised patients
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roy W Sanders, MD
Organizational Affiliation
Florida Orthopaedic Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tampa General Hospital
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to share data at this time.
Learn more about this trial
Humeral Compression/Distraction Device
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