NCT06529601

Brief Summary

The devices compared in this study are 'retainers', i.e. fixed orthodontic retainers applied to the lingual surface of the central and lateral incisors and lower canines bilaterally. Their function is to maintain dental alignment once fixed orthodontic therapy has ended. In particular, the CAD/CAM device Keeppy patented by the company Leone SpA (Via Ponte a Quaracchi 50, Sesto Fiorentino, Florence) will be compared with the standard retainer made from a steel braided wire (Ortho FlexTech, Reliance Orthodontic Products Inc., 1540 West Thorndale Ave, Itasca, Illinois, USA). This is a single-center, national, controlled, superiority, randomized, crossover, open-label study. The aim of this study is to evaluate whether the CAD/CAM retainer results in fewer failures (fractures or detachments) over a period of 6 months and 2 years compared to the standard retainer. In addition, the aim of the study is to evaluate whether the Keeppy device results in the maintenance of better periodontal health as judged by the use of plaque and bleeding indices on the surfaces of the lower six anterior teeth compared to the standard retainer. Other objectives consist of the patient's assessment of pain, difficulty in speaking and esthetic satisfaction and the stability of the lower anterior tooth sector.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
54

participants targeted

Target at P25-P50 for not_applicable

Timeline
17mo left

Started Sep 2024

Typical duration for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress56%
Sep 2024Sep 2027

First Submitted

Initial submission to the registry

July 10, 2024

Completed
21 days until next milestone

First Posted

Study publicly available on registry

July 31, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

September 1, 2024

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2026

Completed
1.6 years until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2027

Expected
Last Updated

July 31, 2024

Status Verified

July 1, 2024

Enrollment Period

1.4 years

First QC Date

July 10, 2024

Last Update Submit

July 29, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Retainer failure at 6-month and 2-year follow-ups

    The primary endpoint is retainer failures at 6-month and 2-year follow-ups. Failure is defined as any complication requiring a retainer repair, in particular total or partial detachment and total or partial fracture.

    At 6 months and at 2 years

Secondary Outcomes (5)

  • Assessment of the plaque and gingival bleeding index at the central and lateral incisors and lower canines.

    At baseline, at 6 months and at 2 years

  • Pain reported by patients

    At baseline, at one month, at 6 months and at 2 years

  • Difficulty in speaking reported by patients

    At baseline, at one month, at 6 months and at 2 years

  • Aesthetic satisfaction reported by patients

    At baseline, at one month, at 6 months and at 2 years

  • Stability of the alignment of the lower anterior teeth

    At 6 months and at 2 years

Study Arms (2)

CAD/CAM mandibular fixed retainer

EXPERIMENTAL
Device: CAD/CAM mandibular fixed retainer

Conventional mandibular fixed retainer

ACTIVE COMPARATOR
Device: Conventional mandibular fixed retainer

Interventions

Keeppy is a Class IIa custom-made medical device manufactured by Digital Service Leone s.r.l. - via Pratese 160/b, Florence, Italy. The Keeppy is an individualized fixed retainer, made of a Nickel-free Chrome Cobalt alloy, produced with a CAD-CAM procedure starting from a digital impression made with an intraoral optical scanner (3 Shape), which allows a perfect adaptation to the lingual surfaces of the 6 lower anterior teeth on which it is bonded. The device is characterized by the presence of applicators that can be placed temporarily on the buccal surface of the canines, which facilitate the clinician in the precise application of the device and which are removed as soon as the bonding phase of the retainer is complete. Bonding is performed using classic composite resins following a preparation phase of the lingual surface of the tooth consisting of the application of etchant (37% orthophosphoric acid) for 30 seconds and adhesive (primer-bonding).

Also known as: Keeppy
CAD/CAM mandibular fixed retainer

The standard control device, which is among the most commonly used in routine clinical practice, consists of a steel braided wire. The device selected for the Class IIa investigation is the Ortho Flex Tech manufactured by Reliance Orthodontic Products, Inc. 1540 West Thorndale Ave. Itasca, IL 60143 USA. The Ortho Flex Tech steel braided wire is manually shaped by the clinician and cut with a wire cutter so that it has the proper length to extend over the 6 dental elements. Once the correct length has been defined, it is then held in place on the lingual surface of the teeth by the use of 2 interdental wires passing doubly through the interdental area (between the lateral incisor and canine on one side and the other). This allows the device to be bonded using composite resin after etching the lingual surfaces of the lower anterior teeth.

Conventional mandibular fixed retainer

Eligibility Criteria

Age13 Years - 20 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Patients who have completed fixed orthodontic therapy between the ages of 13 and 20 years;
  • Patients whose parents will sign the informed consent

You may not qualify if:

  • Presence of dental anomalies in number (excess or deficiency) in the lower anterior teeth
  • Patients with metal allergies.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 10, 2024

First Posted

July 31, 2024

Study Start

September 1, 2024

Primary Completion

February 1, 2026

Study Completion (Estimated)

September 1, 2027

Last Updated

July 31, 2024

Record last verified: 2024-07