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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
  1. Male or female (>18 y)
  2. patient with At least 1 deep carious lesion
  3. Clinical symptoms of reversible pulpitis with positive pulp response
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Exclusion Criteria
    1. 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
GroupInterventionDescription
Zinc modified glass ionomerPartial caries removel techniquesZinc modified glass ionomer (chemfill rock) galss ionomer used as restoration for posterior teeth in case of partial caries removel
Conventionel glass ionomerPartial caries removel techniquesConventional glass ionomer used as restoration for posterior teeth in case of partial caries removel
Primary Outcome Measures
NameTimeMethod
Digital radigraphic assessmentAt baseline ,3months and 6 months

The presence of periapical change or change in lamina dura change after the procedure

Secondary Outcome Measures
NameTimeMethod
Post opreative hypersenstivityBaseline ,at 3 months and at 6 months

The presence or absence of pain with thermal

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