Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT06393699

Restoration of Non-carious Cervical Lesions With Different Resin Composites and Universal Adhesive

Led by Ain Shams University · Updated on 2025-02-27

52

Participants Needed

1

Research Sites

241 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

patients with non carious cervical lesions suffer from dentin sensitivity and presence of cavitations and gingival recession. Restoring these lesions with different composites and evaluation of restorations every 6 months will be done to know the effect of different composite types and consistencies in retention of restorations of such lesions.

CONDITIONS

Official Title

Restoration of Non-carious Cervical Lesions With Different Resin Composites and Universal Adhesive

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 65 years
  • Presence of at least 2 non-carious cervical lesions on one side
  • No medical conditions that interfere with routine dental care
  • Ability to attend all recall visits
  • Healthy periodontal tissues
  • Lesions with no more than 50% of margins in enamel
Not Eligible

You will not qualify if you...

  • Medically compromised patients
  • Pregnant or breastfeeding patients
  • Patients undergoing orthodontic or bleaching treatment during the study
  • Patients with periodontal disease in the target area
  • Patients with fewer than 20 teeth in the mouth
  • Patients without opposing teeth
  • Lesions that are superimposed with caries

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ain shams university

Cairo, Egypt

Actively Recruiting

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Research Team

A

Aisha Elbaz

CONTACT

F

Farid El-Askary

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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