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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

NCT ID: NCT03285022

Last Updated: 2017-09-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

52 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-20

Study Completion Date

2018-04-20

Brief Summary

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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

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The zinc ion has an antibacterial effect which could increase the success of partial caries removel technique by decreasing the bactrial population .

Conditions

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Carious Dentin

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors
Outcome assessor and participant will be blinded to the type of material

Study Groups

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Zinc modified glass ionomer

Zinc modified glass ionomer (chemfill rock) galss ionomer used as restoration for posterior teeth in case of partial caries removel

Group Type EXPERIMENTAL

Partial caries removel techniques

Intervention Type PROCEDURE

Removel of all superfacial dentin and leaving the inner affectted dentin

Conventionel glass ionomer

Conventional glass ionomer used as restoration for posterior teeth in case of partial caries removel

Group Type ACTIVE_COMPARATOR

Partial caries removel techniques

Intervention Type PROCEDURE

Removel of all superfacial dentin and leaving the inner affectted dentin

Interventions

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Partial caries removel techniques

Removel of all superfacial dentin and leaving the inner affectted dentin

Intervention Type PROCEDURE

Other Intervention Names

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Partial caries removel

Eligibility Criteria

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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

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)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Dina mounir elkady

Assisstant lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Dina Mounir Elkady, Assitant lecturer

Role: CONTACT

[email protected]
01004297317

Mohamed Riad Farid, Professor

Role: CONTACT

[email protected]
01223113166

Other Identifiers

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CEBD-CU-2017-09-17

Identifier Type: -

Identifier Source: org_study_id