Clinical Effectiveness of Cobalt Chromium CAD-CAM Designed Customized Lingual Retainer

February 23, 2025 updated by: Hiba Muhammed, University of Baghdad

Clinical Effectiveness of Cobalt Chromium CAD-CAM Designed Customized Lingual Retainer: a Randomized Clinical Trial

This study aims to evaluate the clinical effectiveness of CAD/CAM 3D printed Chrome Cobalt fixed retainer in maintaining mandibular anterior teeth stability.

The Research Question; "Does the Cobalt-Chromium CAD/CAM designed customized lingual retainer better than Stainless steel lingual retainer in improving tooth stability after orthodontic treatment?" The null hypothesis "There is no differences between the fixed CAD/CAM 3D printed Chrome Cobalt customized retainer and the multi-stranded stainless-steel fixed retainer in maintaining mandibular anterior teeth stability."

Study Overview

Detailed Description

A multicenter, single-blinded, randomized controlled trial will be consist of three main parts:

  1. Questionnaire Survey - A cross-sectional survey will be distributed to orthodontists to assess their experience and perception of CAD/CAM retainers.
  2. In Vitro Study - Laboratory tests will be performed on different diameters of CAD/CAM cobalt-chromium retainers to evaluate their mechanical properties, including tensile strength, load deflection, and shear bond strength.
  3. Clinical trial to to evaluate the effectiveness of CAD/CAM retainer group in minimizing the 6month post-orthodontic treatment change in term of a Little's Irregularity Index (LII).

42 Patients will be enrolled; at the last appointment of orthodontic treatment before debonding, subjects will be assessed for the presence of good gingival health parameters using the BPE. Then the patients will have supra gingival debridement followed by an intraoral scan for lower arch; Intraoral scans will be taken for all the participants and STL files will be generated. In addition, a stone model will be made for the lower arch of the control group.

Group 1 (CAD/CAM retainers): STL files will be sent to lab. Group 2 (conventional retainers): The retainer wire will be shaped to adapt passively to the lingual surfaces of lower anterior teeth on the stone model. A silicone transfer key will be prepared to facilitate the positioning of the retainers Laboratory work: CAD/CAM Chrome cobalt retainers; will be digitally designed by the dental technician using EXOCAD software. Then, they will be 3D printed by metal 3D printer and then will be polished. Also, a projection like extensions will be added at the ends of the retainers to avoid slippage in addition to gingivally directed V notch shaped bend in the retainer to increase the retention in the anterior region.

Bonding procedures: The operators will first check the fitting and adaptation of the retainers on the teeth. After cleaning the teeth and isolate them by placement the rubber dam; 35% phosphoric acid etchant gel will be applied. Bonding agent, as the manufacturer's recommendations will be used, After completing the bonding procedure, the patient will be recalled after one week to measure the parameters of gingival health to exclude the plaque retentive fixed appliance effect. The patient will be given oral hygiene instructions and encouraged to use the interdental brush and will be advised to contact the clinician as soon as possible if they have any concerns or problems.

Study Type

Interventional

Enrollment (Estimated)

42

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Baghdad, Iraq, 10071
        • University of Baghdad - College of Dentistry
        • Contact:
        • Contact:
          • Prof. Dr. Ali Mohammed Hameed

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Completion of a course of fixed appliance therapy.
  • with a satisfactory correction of malocclusion and dental alignment.
  • Class I canine relationship based on Andrew's criteria for finishing.
  • Patients with a history of constant oral hygiene measures daily.
  • Good general health.
  • Subjects had a full and normal complement of teeth in the lower labial segments.
  • Teeth within the labial segments should be regularly sized and shaped.
  • Subjects willing to consent to the trial.

Exclusion Criteria:

  • Patients with a deep overbite
  • Patients with traumatic parafunctional habits such as bruxism and clenching.
  • Patients with carious, restored, fractured, or missing lower anterior teeth.
  • Patients with medical health problems that may influence gingival health, like uncontrolled type II diabetic patients.
  • patients under systemic drug administration that affects oral health.
  • Smokers

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: CAD/CAM 3D Printed Chrome Cobalt Fixed Retainers group
The participant will receive a fixed retainer fabricated using computer-aided design and computer-aided manufacturing (CAD/CAM) technology. The retainer will be constructed from cobalt-chromium. The CAD/CAM process involved scanning the patient's dental arch to create a digital model, which was then used to design the retainer. The retainer will be bonded to the lingual surfaces of the mandibular incisors and canines, extending from canine to canine. Participants were instructed to maintain proper oral hygiene and attend regular follow-up appointments.
CAD/CAM Chrome cobalt retainers; will be digitally designed by the dental technician using EXOCAD software. Then, they will be printed by DMP Flex100 metal 3D printer and then will be polished. Also, a projection like extensions will be added at the ends of the retainers to avoid slippage in addition to gingivally directed V notch shaped bend in the retainer to increase the retention in the anterior region
Active Comparator: Stainless steel Fixed Retainer group
participants will receive a fixed orthodontic retainer fabricated from a 0.0215-inch, five-stranded stainless steel wire. The retainer will be bonded to the lingual surfaces of the mandibular incisors and canines, extending from canine to canine. Participants were instructed to maintain proper oral hygiene and attend regular follow-up appointments.
The Stainless steel fixed orthodontic retainer is fabricated from a 0.0215-inch, five-stranded stainless steel wire

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluate the effectiveness of CAD/CAM 3D printed Chrome Cobalt fixed retainers
Time Frame: from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
Evaluate the effectiveness of CAD/CAM 3D printed Chrome Cobalt fixed retainers a in term of post-treatment stability of mandibular anterior teeth over a 6-month period by using Little's Irregularity Index. Post-treatment changes in millimeters will be defined as change in labial segment alignment.
from 1st day of retainer insertion to the last of initial (first ) 6 months of retention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Retainer survival
Time Frame: from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
inter-canine width
Time Frame: from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
the distance between cusp tips of right and left mandibular canines in millimeters.
from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
The pattern of wire failure
Time Frame: from 1st day of retainer insertion to the last of initial (first ) 6 months of retention

The pattern of failure will be recorded:

the wire-composite interface; the enamel-composite interface; wire fracture; or complete detachment from all teeth

from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
overjet
Time Frame: from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
The horizontal distance ( in millimeters) between Maxillary incisor edge labial surface of Mandibular incisors
from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
Overbite
Time Frame: from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
The distance of maximum vertical overlap ( in millimeters) between Maxillary and Mandibular incisors in maximum intercuspation.
from 1st day of retainer insertion to the last of initial (first ) 6 months of retention
assessment of plaque accumulation
Time Frame: after 3 months of retainer insertion to the last of initial (first ) 6 months of retention
by using plaque- disclosing agent and painting all the surfaces of the teeth Plaque index then calculated.
after 3 months of retainer insertion to the last of initial (first ) 6 months of retention
Periodontal Probing Depth.
Time Frame: after 3 months of retainer insertion to the last of initial (first ) 6 months of retention
measured in mm using periodontal prob.
after 3 months of retainer insertion to the last of initial (first ) 6 months of retention
Bleeding on Probing
Time Frame: after 3 months of retainer insertion to the last of initial (first ) 6 months of retention
after 3 months of retainer insertion to the last of initial (first ) 6 months of retention
Patient satisfaction
Time Frame: after 3 months of retainer insertion to the last of initial (first ) 6 months of retention

the patient experience with the new retainer will be evaluated through the Visual Analogue Scale regarding comfort/satisfaction with the Fixed retainers.

There will be five questions relating to how comfortable he/she finds the retainers and how they affect the daily life. Each question must be answered by number from 0 to 100; The left side represents 0 = complete satisfaction/comfort The right side represents 100 = complete discomfort/unsatisfaction

after 3 months of retainer insertion to the last of initial (first ) 6 months of retention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Prof. Dr. Ali Mohammed Hameed, University of Baghdad

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

July 1, 2025

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

December 30, 2026

Study Registration Dates

First Submitted

February 3, 2025

First Submitted That Met QC Criteria

February 19, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 23, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 1021425

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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