Status:
UNKNOWN
Clinical Evaluation of Bulk-fill Alkasite Restoration Versus Resin Modified Glass Ionomer in Adult With Class V Carious
Lead Sponsor:
Cairo University
Conditions:
Cervical Lesion
Eligibility:
All Genders
18-50 years
Phase:
NA
Brief Summary
Cention N will have the same clinical performance as resin-modified glass ionomer in cervical carious lesions. Evaluation of restorations will be done at baseline, six months, and one year according (...
Detailed Description
In this study, Class V carious lesions were restored using two different restorative materials either resin modified glass ionomer or Cention N restorative materials. This study will be held in the re...
Eligibility Criteria
Inclusion
- Inclusion criteria:
- Patients with High caries risk.
- Patients with poor oral hygiene.
- Patients with untreated cervical caries lesion.
- patient aging ≥18 years.
- Absence of tooth mobility
- Absence of abnormal occlusion.
- Patients with good likelihood of recall availability.
- Exclusion criteria:
- Patients with cervical caries lesions need crown restoration.
- Non-vital teeth.
- Evidence of parafunctional habits.
- Teeth supporting removable prosthesis.
- Periapical Abscess or Fistula.
- Patients with systemic disease.
- Patients with xerostomia.
- Participants with a history of allergy to any component of restorations will be used in the study.
Exclusion
Key Trial Info
Start Date :
November 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2022
Estimated Enrollment :
28 Patients enrolled
Trial Details
Trial ID
NCT04716517
Start Date
November 1 2021
End Date
December 1 2022
Last Update
July 28 2021
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