Pain After Buffered Vs Non Buffered Articaine

Part of paid clinical trials in Cleveland, Ohio.

Sponsor
Cleveland Dental Institute
Study ID
NCT06538233
Phase
PHASE2
Status
Recruiting

Conditions

  • Pain

Eligibility Criteria

Sex
ALL
Age
18 Years - 60 Years
Healthy Volunteers
Accepted

Interventions

  • Buffered articaine — DRUG
    Injecting buffered articaine in maxillary anterior region and evaluate pain response.
  • Non buffered articaine — DRUG
    Injecting non buffered articaine in maxillary anterior region and evaluate pain response.

Study Details

Pain after buffered versus non buffered articaine.

Key Dates

Start date
Jan 1, 2024
Status verified
Jul 2024
Primary completion
Oct 31, 2024
Completion
Jan 31, 2025

Study Design

Enrollment
108 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Buffered articaine
  • Active Comparator: non buffered articaine

Primary Outcome Measure

Numerical Rate Scale (NRS) [ Time Frame: Immediate ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Clevland Dental InstituteClevelandOhio44128
Pavanpreet Kaur, Resident
216-355-1155

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