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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05929391
Other study ID # recycling orthodontic
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 1, 2023
Est. completion date March 1, 2024

Study information

Verified date July 2023
Source University of Baghdad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to compare the clinical efficacy of different residual orthodontic adhesive removing methods for rebonding debonded metal attachments.


Description:

1. To evaluate and compare the bond failure rates of rebonded brackets using two methods to remove the adhesive remnant and comparing them with contralateral teeth. 2. To evaluate and compare the bond failure rates of rebonded brackets between different quadrants and arches. 3. To evaluate and compare the bond failure rates of rebonded molar tubes using two methods to remove the adhesive remnant and comparing them with contralateral teeth. 4. To evaluate and compare the bond failure rates of rebonded molar tubes between different quadrants and arches.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 40
Est. completion date March 1, 2024
Est. primary completion date February 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 25 Years
Eligibility Inclusion Criteria: 1. Patients need metal fixed orthodontic appliance treatment; 2. Complete set of permanent dentition with fully erupted teeth on both arches; 3. Intact teeth and mainly their buccal surfaces are free from caries, fillings, or gingival hyperplasia; 4. No occlusal interferences that can affect the ideal position of attachments, especially in the lower arch. Exclusion Criteria: 1. patients have crown, missing teeth, or craniofacial anomalies. 2. patients have congenital enamel defects specially their buccal surface.

Study Design


Related Conditions & MeSH terms

  • Orthodontic Appliance Complication

Intervention

Procedure:
Recycling orthodontic brackets
T0: The adhesive removal will be performed by high-speed hand piece with tungsten carbide bur. the bur will be changed every five attachments. T1: Control group of T0. T2: The adhesive removal will be performed by sandblasting via Micro-etcher. T3: Control group of T2.

Locations

Country Name City State
Iraq 2 private dental clinics in Iraq and special center in Karbala. Baghdad.

Sponsors (1)

Lead Sponsor Collaborator
University of Baghdad

Country where clinical trial is conducted

Iraq, 

References & Publications (3)

Ahmed T, Rahman NA, Alam MK. Assessment of in vivo bond strength studies of the orthodontic bracket-adhesive system: A systematic review. Eur J Dent. 2018 Oct-Dec;12(4):602-609. doi: 10.4103/ejd.ejd_22_18. — View Citation

Alessandri Bonetti G, Zanarini M, Incerti Parenti S, Lattuca M, Marchionni S, Gatto MR. Evaluation of enamel surfaces after bracket debonding: an in-vivo study with scanning electron microscopy. Am J Orthod Dentofacial Orthop. 2011 Nov;140(5):696-702. doi: 10.1016/j.ajodo.2011.02.027. — View Citation

Eminkahyagil N, Arman A, Cetinsahin A, Karabulut E. Effect of resin-removal methods on enamel and shear bond strength of rebonded brackets. Angle Orthod. 2006 Mar;76(2):314-21. doi: 10.1043/0003-3219(2006)076[0314:EORMOE]2.0.CO;2. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The number of bonding failures will be compared using the chi-square test. evaluate and compare the bond failure rates. different quadrants and arches.To evaluate and compare the bond failure rates of rebonded attachments(brackets and molar tubes)using two methods (Tungsten carbide bur and sandblasting)) to remove the adhesive remnant and comparing them with contralateral teeth. baselines
Secondary The bonding failure between each quadrant will be compared by one way ANOVA. evaluate and compare the bond failure rates. different quadrants and arches. bsaelines
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