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Relapse and Failure Rates Between CAD/CAM and Conventional Fixed Retainers

Relapse and Failure Rates Between CAD/CAM and Conventional Fixed Retainers: A 2-year Follow-up of a Randomized Controlled Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05915273
Enrollment
43
Registered
2023-06-22
Start date
2019-09-01
Completion date
2022-09-30
Last updated
2023-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapse

Brief summary

The aim of this study was to compare the differences in relapse and failure rates in patients treated with fixed retainers (FRs) using Computer-Aided Design/Computer-Aided Manufacturing technology, lab-based technique, and chairside method.

Interventions

OTHERLab-based Retainers

The lab group used the same type of wire as the CAD/CAM group but was manually bent by a lab technician

OTHERComputer Aided Design/ Computer Aided Manufacturing Retainers

Custom-bent fixed retainer wires from an in-office CAD/CAM system with FixR software and the BenderI machine (YOAT Corporation, Lynwood, WA). Dentaflex wires- round, 0.5mm in diameter, three-stranded Stainless Steel (Dentaurum GmbH & Co., Ispringen, Germany)- were used for the CAD/CAM group

OTHERChairside Retainers

The chairside group used three-stranded Stainless Steel, 0.974mm x 0.402 mm, flexible Ortho-FlexTech wires (Reliance, Itasca, IL)

Sponsors

Nourhan M.Aly
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
13 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* completion of comprehensive orthodontic treatment * class I molar and canine relationships * indication for a fixed retainer on the mandibular anterior teeth. * no extractions done as part of their treatment. * Treatment with preadjusted edgewise appliance.

Exclusion criteria

* refusal to participate * refusal to have fixed retainers * poor oral hygiene * non-compliance

Design outcomes

Primary

MeasureTime frameDescription
Change in intercanine width (ICW)2 yearsICW was measured on the Meshlab software using the 3D ruler measurement tool. Pre-treatment, post-treatment, and post-retention measures were recorded and any change in the ICW was considered relapse.
Change in Little's Irregularity Index (LII)2 yearsICW was measured on the Meshlab software using the 3D ruler measurement tool. Pre-treatment, post-treatment, and post-retention measures were recorded and any change in the LII was considered relapse.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026