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Essix Retainer vs Hawley Retainer

PHASE 3 STUDY OF THE EFFECTIVITY OF TWO RETAINERS IN THE DENTAL AND OCCLUSAL STABILITY

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01583933
Acronym
retainer
Enrollment
46
Registered
2012-04-24
Start date
2011-09-30
Completion date
2012-05-31
Last updated
2012-04-27

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

Conditions

Dental and Occlusal Stability

Keywords

Dental stability, Occlusal stability, Retainers

Brief summary

There are several factors involved in the decision and the retention plan, such as occlusion, patient age, etiology of malocclusion, the speed of the correction, the length of the cusps and health of the tissues involved, relationships inclined planes, size of the arches, harmony of the arches, muscle pressure, interdental proximal contact, cell metabolism and atmospheric pressure. Given these concepts, we need to find grounds to enable decision making with respect to the retainer that offers the best features of containment and stability.

Detailed description

This study aims to assess the stability of tooth position and occlusal retention during treatment with two types of retainers, Essix type retainer and the retainer plate type Hawley in individuals who have completed their growth ending orthodontic treatment at the Faculty of Dentistry University of Antioquia and CES University Medellín

Interventions

The essix retainer is made in a thermoforming copolyester 0.75mm (0.30 , it processed gives a thickness of 0.015 approximately. Retainer will be used molar to molar. subjects in this arm will have this retainer for 24 hours a day for 6 months, they won´t have this device for food intake.

DEVICEHawley retainer

subjects in this arm will have the retainer for 24 hours a day for 6 months. During food intake they won´t have this device.

Sponsors

Universidad de Antioquia
CollaboratorOTHER
CES University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Patients who have stabilized their growth between 16 and 40 who have completed orthodontic treatment and initiate retention treatment * Who have agreed to participate in the study if elected and to sign informed consent * Residing in the metropolitan area of Medellin and have the opportunity to attend recall appointments

Exclusion criteria

* Periodontal status deteriorated * missing teeth * Cleft lip and palate * History of orthognathic surgery * History of dental or skeletal open bite * Presence of some habit oral tongue thrusting, mouth breathing, thumb sucking even after termination of orthodontic treatment

Design outcomes

Primary

MeasureTime frameDescription
Dental stabilityUp to 6 monthsDental stability will be assessed like this, models: rotation of central and lateral incisor, canine, first and second premolar, first molar on each side and each arch; and cephalometric analysis: SN-upper central incisive, FK-upper central incisive, palate plane-upper central incisive, interincisal angle, mandibular plane-lower central incisive; vertical distances: palate plane-upper central incisive, palate plane-first upper molar, mandibular plane-lower central incisive, mandibular plane-first lower molar; horizontal distances: A-Pogonion upper and lower central incisive.

Secondary

MeasureTime frameDescription
Occlusal stabilityUp to 6 monthsOcclusal stability will be measured at the beginning and end of study through clinic exam and study models. Clinic exam: canine relations right and left, molar relations left and right, overjet, overbite, presence of anterior open bite, presence of posterior open bite. Models: upper and lower arch, upper and lower intercanine distance, upper and lower distance interpremolar, upper and lower intermolar distance.

Countries

Colombia

Contacts

Primary ContactSandra Gómez, Orthodontist
sandraligomez11@gmail.com574 3127492
Backup ContactAngela María Segura Cardona, PhD in Epidemiology
asegura@ces.edu.co574 4440555

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026