Anterior Resin Bonded Restorations for Adolescent

Not Applicable

Active, not recruiting

• Conditions: Missing Teeth

• 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

Study Timeline

• Study First Submitted: 2022-04-23
• Study First Submitted QC: 2022-04-30
• Study First Posted: 2022-05-05
• Study Start: 2022-05-08
• Status Verified: 2024-04
• Last Update Submitted: 2024-04-02
• Last Update Posted: 2024-04-03
• Primary Completion: 2024-05-04
• Study Completion: 2024-06-01

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

Primary Outcome Measures

Name	Time	Method
resin bonded bridge retention/survival	12 month	Presence of the prosthesis in patient's mouth (Yes/No) by clinical visual examination.

Secondary Outcome Measures

Name	Time	Method
Patient's satisfaction	12 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