Postoperative Hypersensitivity and Digital Radiographic Assessment of a Zinc Modified Versus a Conventional Glass Ionomer Cement in Deep Carious Lesion: Randomized Controlled Clinical Trial
Not Applicable
- Conditions
- Carious Dentin
- Interventions
- Procedure: Partial caries removel techniques
- Registration Number
- NCT03285022
- Lead Sponsor
- Cairo University
- Brief Summary
The study aim to evaluate the difference between the effect of zinc modified glass ionomer and conventional glass ionomer on the success of partial caries removel technique
- Detailed Description
The zinc ion has an antibacterial effect which could increase the success of partial caries removel technique by decreasing the bactrial population .
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 52
Inclusion Criteria
- Male or female (>18 y)
- patient with At least 1 deep carious lesion
- Clinical symptoms of reversible pulpitis with positive pulp response
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Exclusion Criteria
-
- Patient suffer from irreversible pulpitis (pain with hot or instant pain lasting for a while, resistant to analgesic) 2. Presence of any sign of periapical lesion (like sinus tract ) 3. Teeth with periodontal problem 4. Anterior teeth (material used for non aesthetic region) 5. Pregnant women, to avoid multiple exposure to x ray 6. Patients unable to give consent(mentally retarted, or refuse to right a consent)
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Zinc modified glass ionomer Partial caries removel techniques Zinc modified glass ionomer (chemfill rock) galss ionomer used as restoration for posterior teeth in case of partial caries removel Conventionel glass ionomer Partial caries removel techniques Conventional glass ionomer used as restoration for posterior teeth in case of partial caries removel
- Primary Outcome Measures
Name Time Method Digital radigraphic assessment At baseline ,3months and 6 months The presence of periapical change or change in lamina dura change after the procedure
- Secondary Outcome Measures
Name Time Method Post opreative hypersenstivity Baseline ,at 3 months and at 6 months The presence or absence of pain with thermal