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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05812066
Other study ID # 2-1-23
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 1, 2023
Est. completion date February 28, 2025

Study information

Verified date April 2023
Source Cairo University
Contact mohamed A belead, master
Phone 01124741165
Email mohamed-belead@dentistry.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Intervention Will be All Ceramic Single-retainer Resin Bonded Fixed Partial Denture Using the Upper Canine as Abutment With Minimum Preparation on the Lingual Surface Within the Enamel Providing Maximum Area for the Retainer Bonding, to Replace the Upper Lateral Incisor and Will be Compared With the Control/Comparator Group Which is the All Ceramic Single-retainer RBFPD Using the Upper Central Incisor. The Participants in This Study Will be Recruited by the Researcher From the Clinic of Fixed Prosthodontics Department, Clinic of Orthodontics Department and Clinic of Diagnosis Department, Cairo University Without Any Financial or Non-financial Incentives.


Description:

The intervention will be all ceramic single-retainer Resin Bonded Fixed Partial Denture using the upper canine as abutment with minimum preparation on the lingual surface within the enamel providing maximum area for the retainer bonding, to replace the upper lateral incisor and will be compared with the control/comparator group which is the all ceramic single-retainer RBFPD using the upper central incisor. This intervention will be done by one investigator in all study groups who has master degree in fixed prosthodontics with eight years of experience. The intervention will be carried out in the clinic of the department of Fixed Prosthodontics, Cairo University under supervision of PhD holder staff members. The self-adhesive dual cure resin cement will be used for cementation in all groups. In the first session, the participant will be informed about all steps from the beginning to the end. All participants will be encouraged to maintain good oral hygiene and attend the regular follow up visits and in case of any complain related to the investigated restoration.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 54
Est. completion date February 28, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 14 Years to 30 Years
Eligibility Inclusion Criteria: - Patients who have unilateral or bilateral missing upper lateral incisor and need to replace them with the following criteria: - From 14-30 years old and be able to read and sign the informed consent document. - physically and psychologically able to withstand conventional dental procedure - Sound or minimally restored abutment with enough enamel surface area for bonding and no periodontal diseases. - If the patient had previously undergone orthodontic treatment, a stabilization period of at least 3 months before impression taking. - Good oral hygiene. - Able to return for follow-up examinations and evaluation. - No signs and symptoms of bruxism. Exclusion Criteria: - Pregnant women - Increased overbite - Bruxism, clenching or abnormal habits like nail or pencil biting that create occlusal forces - Any developmental anomaly affecting the enamel of upper central incisor or canine - Uncontrolled caries and periodontal disease and uncooperative patients. 6- Medically unfit for dental treatment and follow up.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
all ceramic single-retainer resin bonded fixed partial denture
The intervention will be all ceramic single-retainer RBFPD using the upper canine as abutment with minimum preparation on the lingual surface within the enamel providing maximum area for the retainer bonding, to replace the upper lateral incisor and will be compared with the control/comparator group which is the all ceramic single-retainer RBFPD using the upper central incisor.

Locations

Country Name City State
Egypt Faculty of Dentistry, Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival rate in the term of De-bonding and fracture the de-bonding and fracture of the restoration of the two groups will be examined using Binary measurement ( de-bonding or fracture= Yes while no de-bonding and no fracture= No). 12 months
Secondary Abutment tooth mobility and patient's satisfaction the mobility of abutment teeth will be checked using Periotest while the patient's satisfaction will be examined using the questionnaire form containing 10 score ( number 1 denoting most satisfied while number 10 denote the least satisfied; (from 1 to 5 will be considered as satisfied while from 6 to 10 will be considered as unsatisfied). 12 months
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