Status
Conditions
Treatments
About
A crossover study will be conducted on 20 pediatric patients aged 7-11 years. For each participant, the upper and lower study models will be processed using two methods: the conventional method, which involves alginate impressions, and the digital method, which utilizes a 3D intraoral digital scanner (CEREC Omnicam scanner or equivalent). Measurements of arch length, arch width, and arch depth will be taken from both model types using the conventional method with a brass wire and a digital caliper. At the same time, in the scan cast, they will be calculated digitally by 3D shape software. Statistical analysis will be done to compare the results of both methods.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
20 participants in 2 patient groups
Loading...
Central trial contact
Nehal Raid Salman, Lecturer
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal