Anterior Resin Bonded Restorations for Adolescent

N/AActive Not RecruitingNCT05362591

October University for Modern Sciences and Arts24 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Missing Teeth

Interventions

resin bonded bridge with no preparationPROCEDURE

resin bonded bridge without enamel preparation

resin bonded bridge with minimal preparationPROCEDURE

resin bonded bridge with minimal preparation of tooth enamel

Eligibility

Sex: ALLMin age: 12 YearsMax age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (1)

October university for modern sciences and arts

Cairo, Egypt

Outcomes

Primary Outcomes

resin bonded bridge retention/survival

Presence of the prosthesis in patient's mouth (Yes/No) by clinical visual examination.

Time frame: 12 month

Secondary Outcomes

Patient's satisfaction

Patient 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).

Time frame: 12 month

Data from ClinicalTrials.gov

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