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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
Florida Orthopaedic Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Humeral Fractures focused on measuring upper extremity fracture

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
August 3, 2016
Last Updated
September 5, 2018
Sponsor
Florida Orthopaedic Institute
Collaborators
NuVasive, St. Louis University
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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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