A Commercial Available Tooth Positioner for the Treatment of Simple Orthodontic Relapse (NCT03332082) | Clinical Trial Compass
WithdrawnNot Applicable
A Commercial Available Tooth Positioner for the Treatment of Simple Orthodontic Relapse
Stopped: losing of funding for the study
0Started 2019-01
Plain-language summary
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.
Who can participate
Age range18 Years – 60 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Permanent dentition
✓. Class I malocclusion with crowding or spacing of less than 6 mm for mandibular or maxillary incisors, lower number 1's through 3's
✓. Predicted compliance with device use, as determined by the investigator orthodontist
✓. Good oral hygiene, as determined by the investigator orthodontist
✓. At least average intelligence, as determined by investigator orthodontist
Exclusion criteria
✕. Any medical or dental condition that in the opinion of the investigator could impact study results during the expected length of the study
✕. Patient is currently using any investigational drug or any other investigational device
✕. Patient plans to relocate or move within six months of enrollment
✕. Allergic to acetaminophen (use of aspirin or non-steroidal anti-inflammatory drugs is excluded for patients while on the study)
What they're measuring
1
The Little's Index
Timeframe: 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.