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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02283528
Other study ID # IRB00076048
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2015
Est. completion date December 21, 2017

Study information

Verified date January 2019
Source Emory University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients who sustain a fracture of the lower jaw are typically treated by wiring the teeth together or using small titanium plates and screws to fix the fracture. With either technique the upper and lower teeth are held together to ensure that the fracture is held in the correct position during healing (for closed reduction) or while the plate and screws are applied (for open reduction).

The teeth can be held together using Erich arch bars which are a type of braces that are temporarily wired to the existing teeth. These stay in place for 6 weeks until the fracture has healed even though the patient is able to open his mouth immediately after the surgery is complete. The alternative to the traditional Erich arch bars is a relatively new type of arch bar (Stryker Hybrid) that is screwed to the jaw bone rather than wired to the teeth. The purpose of this study is to compare the two types of arch bars in terms of the speed with which they can be applied as well as any difference in fracture healing


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 21, 2017
Est. primary completion date December 21, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Mandible fracture involving subcondyle, ramus, angle, body, parasymphysis and symphysis

2. Age 18 years - 90 years

3. Ability to give informed consent

4. Minimum 6 weeks follow-up

5. Pre and post-operative panoramic xrays

Exclusion Criteria:

1. Comminuted fractures

2. Infected fractures

3. Previously treated fractures

4. Complete edentulism

5. Gun shot wounds

6. Pregnancy or breast feeding

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Stryker Hybrid
Place Hybrid arch bars
Erich
Control group is Erich arch bars

Locations

Country Name City State
United States Grady Memorial Hospital Atlanta Georgia

Sponsors (1)

Lead Sponsor Collaborator
Emory University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to Place Archbars Time taken to place archbars During initial admission and surgery
Secondary Number of Participants With Fracture Healing at 6 Weeks Radiographic healing 6 weeks
Secondary Number of Participants With Complications Including Loosening of Archbars, Loosening of MMF, or Damage to Adjacent Teeth and Structures assess operative and post-operative complications to include loosening of archbars, loosening of MMF if stratified to closed reduction and damage to adjacent teeth and structures up to 6 weeks post operatively
See also
  Status Clinical Trial Phase
Recruiting NCT03466190 - Clinical Assessment of Computer-assisted PEEK Versus Conventional Titanium Plates on Mandibular Body Fractures N/A