Status:
COMPLETED
Evaluation of Post-operative Sensitivity of Bulk Fill Resin Composite Versus the Nano Resin Composite.
Lead Sponsor:
Rasmia Mamdouh Ali Salem
Collaborating Sponsors:
World Health Organization
Conditions:
Sensitivity
Eligibility:
All Genders
25-40 years
Phase:
NA
Brief Summary
Our study evaluated and compared the postoperative sensitivity of the placement technique (incremental and bulk fill) in class II posterior composite resin restorations bonded with two different adhes...
Detailed Description
Our results revealed that when the two composite types using self-etch adhesive system \& total-etch adhesive system were evaluated; there was no statistically significant difference between the two c...
Eligibility Criteria
Inclusion
- Patients must show no signs of spontaneous dental or orofacial pain.
- The presence of molar and premolar class II teeth requiring composite restorations for the treatment of primary carious lesions
- The selected teeth should have an occlusal contact with natural or crowned antagonist teeth
- The selected teeth should have a proximal contact with the adjacent teeth.
- Shallow and mid-sized cavity depths will be included in the study .
Exclusion
- Increasing pre-operative sensitivity of the selected teeth.
- Teeth with abnormal periapical anatomy or caries that will be likely to result in very deep restorations.
- Teeth with old restorations or severely destructed dental crowns.
- Teeth with spontaneous pain
- Tempro-mandibular joint problems involving symptomatic pain.
- Patients taking analgesics that could alter their normal pain perception level.
- Pregnancy or breast feeding, acute and chronic systemic diseases, immunecompromised patients.
Key Trial Info
Start Date :
September 1 2016
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 25 2017
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT03792178
Start Date
September 1 2016
End Date
April 25 2017
Last Update
January 7 2019
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