MedPath

Anterior Resin Bonded Restorations for Adolescent

Not Applicable
Active, not recruiting
Conditions
Missing Teeth
Interventions
Procedure: resin bonded bridge with no preparation
Procedure: resin bonded bridge with minimal preparation
Registration Number
NCT05362591
Lead Sponsor
October University for Modern Sciences and Arts
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
24
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
resin bonded bridge with no preparationresin bonded bridge with no preparationresin bonded bridge without enamel preparation
resin bonded bridge with minimal preparationresin bonded bridge with minimal preparationresin bonded bridge with minimal preparation on tooth enamel
Primary Outcome Measures
NameTimeMethod
resin bonded bridge retention/survival12 month

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

Secondary Outcome Measures
NameTimeMethod
Patient's satisfaction12 month

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).

Trial Locations

Locations (1)

October university for modern sciences and arts

🇪🇬

Cairo, Egypt

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