Orthodontics Clinical Trial
Official title:
A Clinical Trial on the Use of a Commercial Available Tooth Positioner for the Treatment of Simple Orthodontic Relapse
Verified date | March 2019 |
Source | University of Alabama at Birmingham |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Orthodontic relapse occurs in almost 80% of Orthodontic Treatment. The only prevention to
phenomenon is the use of fixed retainers or life time active retention. Unfortunately,
patients do not comply and after a year of treatment, many stop wearing their retainers and
Orthodontic relapse occurs.
The aim of this project is to prospectively analyze the treatment result of consecutive
treated patients who have had active orthodontic relapse. 20 patients will be recruited
through advertisement to the Department of Orthodontics at the University of Alabama at
Birmingham (UAB). The sample will comprise of 20 patients with Class I malocclusions. The
records to be collected will comprise of clinical pictures and pre and post study casts. The
3D study casts will be evaluated using the Little's Index. The results will be analyzed with
the paired t-test and ANOVA, using the Statistical Analysis System (SAS/STAT®) software.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2019 |
Est. primary completion date | November 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: 1. Permanent dentition 2. Class I malocclusion with crowding or spacing of less than 6 mm for mandibular or maxillary incisors, lower number 1's through 3's 3. Predicted compliance with device use, as determined by the investigator orthodontist 4. Good oral hygiene, as determined by the investigator orthodontist 5. At least average intelligence, as determined by investigator orthodontist Exclusion Criteria: 1. Any medical or dental condition that in the opinion of the investigator could impact study results during the expected length of the study 2. Patient is currently using any investigational drug or any other investigational device 3. Patient plans to relocate or move within six months of enrollment 4. Allergic to acetaminophen (use of aspirin or non-steroidal anti-inflammatory drugs is excluded for patients while on the study) 5. Use of bisphosphonates, such as osteoporosis drugs, during the study 6. Pregnancy |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Alabama at Birmingham |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Little's Index | The Little's Index of Displacement score will be the primary clinical endpoint used to judge patient success (i.e., effectiveness). | Movement will be recorded by capturing the start and end point of the 6 anterior teeth before and at the completion of the treatment respectively. The duration of the treatment will be up to 10 months. |
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