The Efficacy of Lingual Aligners in Adults.

NCT ID: NCT06050655

Last Updated: 2024-10-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-09-19

Study Completion Date

2025-08-31

Brief Summary

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The goal of this clinical trial is to test the effectiveness of lingual aligners in adults.

The main question to answer is:

\- Are lingual aligners effective in achieving desired and predicted tooth movements?

Detailed Description

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The aim of this pilot study is to assess the effectiveness and the accuracy of lingual aligners by evaluating the discrepancy between the predicted and the achieved amounts of tooth movements.

Also:

* Patient discomfort and pain
* Appliance defects
* Patient compliance
* Chair and treatment time

Key inclusion criteria:

* Adults older than 18 years old
* About to undergo orthodontic treatment

Key exclusion criteria:

* Patients with tooth extractions or tooth agenesis with space closure
* Patients with surface enamel defects
* Pregnant patients
* Syndromic patients or those with cleft lip and/or palate
* Patients with metabolic diseases

Conditions

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Malocclusion, Angle Class I

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Adults with Angle Class I malocclusion

* Adults older than 18 years old
* About to undergo orthodontic treatment

Group Type EXPERIMENTAL

Lingual aligners

Intervention Type DEVICE

orthodontic treatment with lingual aligners

Interventions

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Lingual aligners

orthodontic treatment with lingual aligners

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Adults older than 18 years old
* About to undergo orthodontic treatment

Exclusion Criteria

* Patients with tooth extractions or tooth agenesis with space closure
* Patients with surface enamel defects
* Pregnant patients
* Syndromic patients or those with cleft lip and/or palate
* Patients with metabolic diseases
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Geneva

OTHER

Sponsor Role lead

Responsible Party

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Fabiana Mutzenberg

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University of Geneva

Geneva, Canton of Geneva, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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2023-D0045

Identifier Type: -

Identifier Source: org_study_id

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