Biomimetic Anterior Resin Bonded Restorations for Adolescent Patients
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Enrollment
- 24
- Locations
- 2
- Primary Endpoint
- resin bonded bridge retention/survival
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Outcomes Assessor)
Eligibility Criteria
- Ages
- 12 Years to 18 Years (Child, Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •12-18 years old
- •Full set of permanent teeth.
- •Missing upper incisor
- •Controlled dental disease - no active caries or periodontal diseases
- •Patients will be available to be clinically reviewed up to 1 year
Exclusion Criteria
- •Patients with uncontrolled active tooth decay or periodontal disease (i.e. 4+ mm probing depth and bleeding on probing).
- •Patients with teeth missing opposite to the planned RBB
- •Abutment tooth mobility of 2 or greater (Millers classification)
- •Patients with debilitating illnesses or complicating medical conditions
- •Heavily restored tooth abutment not suitable for an RBB
Outcomes
Primary Outcomes
resin bonded bridge retention/survival
Time Frame: 12 month
Presence of the prosthesis in patient's mouth (Yes/No) by clinical visual examination.
Secondary Outcomes
- Patient's satisfaction(12 month)
Investigators
Naglaa Ibrahim Ezz
Associate professor
October University for Modern Sciences and Arts
