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Comparison of buccal patches containing lidocaine and dexmedetomidine with articaine and dexmedetomidine in dental procedures

Phase 2
Recruiting
Conditions
Pain caused by local anesthetic injection..
Other dental procedure status
Z98818
Registration Number
IRCT20210118050067N2
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
180
Inclusion Criteria

Patients should cooperate for the study.
Visiting for dental services that require local anesthesia.

Exclusion Criteria

Those with any systemic disease (cardiovascular disease, diabetes, etc.), physical and mental illness.
Patients who have a history of taking any painkillers and corticosteroids in the last week.
Patients who have allergy to lidocaine and articaine.
Patients who have dental phobia.
Patients who have inflammation, abscess, and history of surgery at the injection site.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain caused by injection. Timepoint: 20 minutes after lidocaine injection. Method of measurement: After finishing the procedure, we ask the patients to mark the pain they experienced on the Visual Analogue Scale from 0 to 10.
Secondary Outcome Measures
NameTimeMethod
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