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Anterior Resin Bonded Restorations for Adolescent

Biomimetic Anterior Resin Bonded Restorations for Adolescent Patients

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05362591
Enrollment
24
Registered
2022-05-05
Start date
2022-05-08
Completion date
2024-06-01
Last updated
2024-04-03

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

Conditions

Missing Teeth

Keywords

missing incisors, resin bonded bridge

Brief summary

a 24 Patients above 12 years old with missing upper incisor were divided into two groups, group 1: 12 patient will be treated by resin bonded bridge (RBB) with no preparation protocol, group 2: 12 patient will be treated by resin bonded bridge (RBB) with minimal preparation protocol. (RBB) retention/survival, patient's speech as well as thermal sensitivity and patient's satisfaction will be evaluated for 12 month at 3,6,9 and 12 month.

Interventions

PROCEDUREresin bonded bridge with no preparation

resin bonded bridge without enamel preparation

PROCEDUREresin bonded bridge with minimal preparation

resin bonded bridge with minimal preparation of tooth enamel

Sponsors

October University for Modern Sciences and Arts
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

1. 12-18 years old 2. Full set of permanent teeth. 3. Missing upper incisor 4. Controlled dental disease - no active caries or periodontal diseases 5. Patients will be available to be clinically reviewed up to 1 year

Exclusion criteria

1. Patients with uncontrolled active tooth decay or periodontal disease (i.e. 4+ mm probing depth and bleeding on probing). 2. Patients with teeth missing opposite to the planned RBB 3. Abutment tooth mobility of 2 or greater (Millers classification) 4. Patients with debilitating illnesses or complicating medical conditions 5. Heavily restored tooth abutment not suitable for an RBB

Design outcomes

Primary

MeasureTime frameDescription
resin bonded bridge retention/survival12 monthPresence of the prosthesis in patient's mouth (Yes/No) by clinical visual examination.

Secondary

MeasureTime frameDescription
Patient's satisfaction12 monthPatient satisfaction outcome is including the following: comfort and stability, esthetics, ease of cleaning, ability to speak, self-esteem, and functionality. the outcome will be evaluated by a visual analogue scale ranging from 0 to 10, where 10 is the maximum (better outcome) and 0 is the minimum (worse outcome).

Countries

Egypt

Outcome results

None listed

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