Clinical Assessment of Indirect Restoration Fabricated From Nano Hybrid Composite Blocks Versus Ceramic Blocks in Badly Broken Teeth One Year Follow up

Sponsor

Cairo University (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT04563624

Collaborator

(none)

Enrollment

Arms

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

The aim of the study is to compare one-year clinical performance of indirect restoration fabricated from nano hybrid composite CAD CAM blocks and ceramic blocks

Condition or Disease	Intervention/Treatment	Phase
Teeth Restoration	Drug: composite blocks Drug: ceramic cad cam blocks	Phase 1

Detailed Description

This research is conducted for comparing the clinical efficacy of nano hybrid composite blocks and ceramic blocks ., the choice of nano hybrid composite blocks based on the claim of the manufacturer, as it's considered to be promising , nano hybrid composite blocks has the highest fillers content (86% by weight), resembles natural teeth perfectly , Excellent physical values for flexural strength and abrasion, No firing required (a real one step ), can be processed using any conventional milling unit, can be finished and polished optimally, Ideal for grinding even in cases with thin edges.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

42 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Primary Purpose:

Treatment

Official Title:

Clinical Assessment Accourding to Modified Usphs"of Indirect Restoration Fabricated From Nano Hybrid Composite Blocks Versus Ceramic Blocks in Badly Broken Teeth One Year Follow up Randomized Clinical Trial

Anticipated Study Start Date :

Oct 1, 2020

Anticipated Primary Completion Date :

Nov 1, 2020

Anticipated Study Completion Date :

Nov 1, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: ceramic cad cam blocks	Drug: ceramic cad cam blocks ceramic cad cam blocks
Active Comparator: composite cad cam blocks	Drug: composite blocks cad cam composite blocks

Arm

Intervention/Treatment

Experimental: ceramic cad cam blocks

Drug: ceramic cad cam blocks

ceramic cad cam blocks

Active Comparator: composite cad cam blocks

Drug: composite blocks

cad cam composite blocks

Outcome Measures

Primary Outcome Measures

marginal integrity [one year]
using usphs visual inspection

Eligibility Criteria

Criteria

Ages Eligible for Study:

16 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Patients with badly broken vital teeth
Young adult Males or female
Good oral hygiene measures
Cooperative patients approving to participate in the study

Exclusion Criteria:

Patients with a compromised medical history.
Severe or active periodontal disease
Severe medical complications
Lack of compliance
Endodontically treated teeth

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Haneen ahmed shafik elmoselhy, assistant lecturer in the operative department, British University In Egypt

ClinicalTrials.gov Identifier:

NCT04563624

Other Study ID Numbers:

13919991

First Posted:

Sep 24, 2020

Last Update Posted:

Sep 28, 2020

Last Verified:

Sep 1, 2020

Individual Participant Data (IPD) Sharing Statement:

Undecided

Plan to Share IPD:

Undecided

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Tooth Fractures

Study Results

No Results Posted as of Sep 28, 2020