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Recruiting NCT04828096

NCT04828096 Retention With Three Different Bonded Retainers a Multicenter, Randomized Controlled Trial With 5-year Follow-up

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Clinical Trial Summary
NCT ID NCT04828096
Status Recruiting
Phase
Sponsor Region Örebro County
Condition Dental Malocclusion
Study Type INTERVENTIONAL
Enrollment 324 participants
Start Date 2021-03-25
Primary Completion 2026-09-30

Eligibility & Interventions

Sex All sexes
Min Age 10 Years
Max Age 60 Years
Study Type INTERVENTIONAL
Interventions
Orthodontic retention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 324 participants in total. It began in 2021-03-25 with a primary completion date of 2026-09-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

One of major challenges in orthodontics is to inhibit relapse and ensure stability of treatment outcomes. Retention is the phase of orthodontic treatment that attempts to keep teeth in the corrected position after correction with orthodontic braces. Without retention there is a tendency for the teeth to return to their initial position (1). Retention is usually necessary to overcome the elastic recoil of the periodontal supporting fibers and to allow remodeling of the alveolar bone. The bonded orthodontic lingual retainer constructed from composite and orthodontic wires provides an esthetic and efficient system for maintained retention and has been shown to be an effective means of retaining aligned anterior teeth in the post treatment position in the long term. This has been in popular use as a method of retention since the late 1970s (2). The traditional retainers, which are still in use, are multi-strand stainless steel retainers such as Penta-one® 0.0215 (Masel Orthodontics, Carlsbad, CA, USA). The main problem with multistrand stainless steel retainers is their high rate of failure. Clinical studies indicate that 5% to 37% of mandibular retainers fail during retention in some form, either bond failure or wire breakage (3-5). Reliance Orthodontic Products, Inc. (Itasca, IL, USA) recently introduced a bonded retainer system (Ortho-Flextech™ chain). This retainer's bonding is claimed to be quick and easy by reducing chairside time and eliminating laboratory costs (6). One other recently introduced retainer is Memotain™ (CA-Digital in Mettmann, Germany). Memotain is a CAD/CAM fabricated lingual retainer made of 0.014 X 0.014-inch rectangular nickel-titanium. The wire is highly flexible and custom cut to precisely adapt to the patient's lingual tooth anatomy. According to manufacturer, Memotain offers numerous perceived advantages to traditional multistranded lingual wires, including no need for wire measuring or bending, individually optimized placement, greater accuracy of fit, tighter interproximal adaptation, less tongue irritation, better durability, and resistance to microbial colonization (6). However, randomized clinical trials are necessary to determine whether these advantages are substantiated with scientific data. A recent review by the Cochrane group concluded that to date there is insufficient evidence to single out any particular retention strategy as the preferred method: it was recommended that future studies should include true randomization, reporting of dropouts, adequate sample size calculation, and a minimum follow-up period of 3 months (8). Thus, the aims of this multicenter, randomised controlled trial are: * To compare and evaluate the effectiveness and failure rate of Penta-one multistrand, Ortho-Flextech and Memotain retainers with each other * To compare the possible complications between the three retainers over time * To establish the cost-effectiveness of the three retainers * To evaluate the effectiveness of sandblasting in the retention of the wires

Eligibility Criteria

Inclusion Criteria: * Patients requiring mandibular lingual fixed canine-to-canine retainer after undergoing orthodontic treatment with fixed appliances * Sound enamel on the lingual surface * Calculus-free lingual surface in the lower anterior segment Exclusion Criteria: \-

Contact & Investigator

Central Contact

Farhan Bazargani, DDS, PhD

✉ farhan.bazargani@regionorebrolan.se

📞 +46196024050

Frequently Asked Questions

Who can join the NCT04828096 clinical trial?

This trial is open to participants of all sexes, aged 10 Years or older, up to 60 Years, studying Dental Malocclusion. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04828096 currently recruiting?

Yes, NCT04828096 is actively recruiting participants. Contact the research team at farhan.bazargani@regionorebrolan.se for enrollment information.

Where is the NCT04828096 trial being conducted?

This trial is being conducted at Barcelona, Spain, Örebro, Sweden.

Who is sponsoring the NCT04828096 clinical trial?

NCT04828096 is sponsored by Region Örebro County. The trial plans to enroll 324 participants.

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