- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07716007
Bone Level Changes Using Clear Aligners Compared to Fixed Appliances in Non-Extraction Treatment of Adults
Evaluation of Bone Level Changes Using Clear Aligners Compared to Fixed Appliances in Non-extraction Treatment of Adult Patients: A Randomized Clinical Trial
This study compares two common ways of straightening teeth in adults who have mild-to-moderate crowding of the lower front teeth and do not need any teeth removed: clear aligners and traditional fixed braces.
The main aim is to find out whether the two methods differ in how they affect the bone that surrounds the teeth. Using three-dimensional X-ray scans (cone-beam CT) and digital models of the teeth taken before and during treatment, the researchers measure the level and thickness of the bone around the lower front teeth, the tilt (inclination) of the lower front teeth, and how quickly the crowding is corrected.
Adults are randomly assigned to receive either clear aligners or fixed braces, and the same measurements are compared between the two groups over about six months.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Cairo, Egypten, 11865
- Faculty of Oral and Dental Medicine, Future University in Egypt (Department of Orthodontics)
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Adults 18-25 years of age, of both sexes.
- Mild-to-moderate mandibular anterior crowding (2-6 mm).
- Angle Class I molar relationship with normal overjet (1-3 mm) and overbite (1-2 mm).
- Full permanent dentition with a healthy periodontium.
- Normal anteroposterior and vertical skeletal pattern.
Exclusion Criteria:
- Any local or systemic condition, or trauma, capable of affecting craniofacial growth and development.
- History of previous orthodontic or interceptive treatment.
- Loss of periodontal attachment.
- Craniofacial anomalies, facial asymmetry or skeletal discrepancy.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Fixed appliances (Group FA)
Conventional pre-adjusted edgewise fixed appliance (0.022-inch slot, MBT prescription) bonded from first molar to first molar; levelling and alignment with a sequence of nickel-titanium and stainless-steel archwires over approximately six months.
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Brackets bonded first-molar-to-first-molar; alignment sequence 0.014" NiTi → 0.016" NiTi → 0.016 × 0.022" NiTi → 0.017 × 0.025" stainless steel.
Interproximal reduction performed on assigned contacts where indicated.
Andre navne:
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Eksperimentel: Clear aligners (Group CA)
Three-dimensionally printed, thermoformed clear aligners with bonded attachments and interproximal reduction as indicated; worn ~22 hours/day and changed per the digital staging, with clinical review every four weeks over approximately six months
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Digital intraoral scan and staging (3Shape Ortho Analyzer); 3D-printed models thermoformed into aligners; attachments bonded where planned; sequential aligners worn ~22 h/day.
Interproximal reduction per contact from canine-to-canine is done.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Change in alveolar bone level
Tidsramme: Baseline (T0) and end of alignment phase (T3)) (approximately 6 months)
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Change (mm) in the distance from the cemento-enamel junction to the alveolar crest on the labial and lingual aspects of the mandibular central incisors, lateral incisors and canines, measured on CBCT (OnDemand software), calculated as the difference between baseline and end-of-alignment values.
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Baseline (T0) and end of alignment phase (T3)) (approximately 6 months)
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Change in alveolar bone thickness
Tidsramme: Baseline (T0) and end of alignment phase (≈ 6 months)
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Change (mm) in labial and lingual alveolar bone thickness measured at 3 mm and 6 mm from the CEJ and at the root apex of the mandibular central incisors, lateral incisors and canines on CBCT (OnDemand software), from baseline to end of alignment.
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Baseline (T0) and end of alignment phase (≈ 6 months)
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Change in mandibular incisor inclination (torque)
Tidsramme: Baseline (T0) and end of alignment phase (≈ 6 months)
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Change (degrees) in the inner angle between the long axis of each mandibular central incisors, lateral incisors and canines and the mandibular plane, measured on the sagittal view of CBCT (Invivo/Anatomage software), from baseline to end of alignment.
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Baseline (T0) and end of alignment phase (≈ 6 months)
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Rate of alignment (Little's Irregularity Index)
Tidsramme: Baseline (T0), 8 weeks (T1), 16 weeks (T2) and end of alignment (T3, ≈ 24 weeks / 6 months)
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Reduction in mandibular anterior crowding quantified by Little's Irregularity Index (mm) - the sum of the displaced anatomic contact points from canine to canine - measured on serial digital models; the change across time points and the percentage improvement from baseline describe the rate of alignment.
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Baseline (T0), 8 weeks (T1), 16 weeks (T2) and end of alignment (T3, ≈ 24 weeks / 6 months)
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Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: ahmed mohamed hesham elzoghary, Faculty of Oral and Dental Medicine, Future University in Egypt
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- FUE.REC (18)/7-2024
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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