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Purpose

Pain after buffered versus non buffered articaine.

Condition

Eligibility

Eligible Ages
Between 18 Years and 60 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Males and females, age- 18 to 60 yrs. - Medically free. - Need a dental treatment in the upper anterior region.

Exclusion Criteria

  • Periodontally affected teeth. - Radiographic bone loss. - Upnormal length of the teeth.

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Buffered articaine
  • Drug: Buffered articaine
    Injecting buffered articaine in maxillary anterior region and evaluate pain response.
Active Comparator
non buffered articaine
  • Drug: Non buffered articaine
    Injecting non buffered articaine in maxillary anterior region and evaluate pain response.

Recruiting Locations

Clevland Dental Institute
Cleveland, Ohio 44128
Contact:
Pavanpreet Kaur, Resident
216-355-1155
p.kaur@cdiohio.org

More Details

Status
Recruiting
Sponsor
Cleveland Dental Institute

Study Contact

Pavanpreet Kaur, Resident
2163551155
p.kaur@cdiohio.org

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.