Study Results
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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RECRUITING
PHASE2
108 participants
INTERVENTIONAL
2024-01-01
2025-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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Buffered articaine
Buffered articaine
Injecting buffered articaine in maxillary anterior region and evaluate pain response.
non buffered articaine
Non buffered articaine
Injecting non buffered articaine in maxillary anterior region and evaluate pain response.
Interventions
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Buffered articaine
Injecting buffered articaine in maxillary anterior region and evaluate pain response.
Non buffered articaine
Injecting non buffered articaine in maxillary anterior region and evaluate pain response.
Eligibility Criteria
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Inclusion Criteria
* Medically free.
* Need a dental treatment in the upper anterior region.
Exclusion Criteria
* Radiographic bone loss.
* Upnormal length of the teeth.
18 Years
60 Years
ALL
Yes
Sponsors
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Cleveland Dental Institute
OTHER
Responsible Party
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Principal Investigators
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Ahmed H Khalifa, PhD
Role: STUDY_CHAIR
Cleveland Dental Institute
Waleed Elmallah, PhD
Role: PRINCIPAL_INVESTIGATOR
Cleveland Dental Institute
Locations
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Clevland Dental Institute
Cleveland, Ohio, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CDIOS00010
Identifier Type: -
Identifier Source: org_study_id
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