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Comparison of the effect of local pressure and topical anesthesia with lidocaine /prilocaine cream (EMLA) on pain during infiltration of maxillary canine teeth: Randomized clinical trial

Phase 3
Conditions
local anesthesia.
Codes for special purposes
Registration Number
IRCT2015120925456N1
Lead Sponsor
Dental and Periodontal Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
140
Inclusion Criteria

Healthy adults with the age 18-55 years old; intact or with minimal caries and restoration maxillary canine teeth with normal view in periapical radiography; normal probing depth; no sensitivity to palpation and percussion; no consumption of painkillers,analgesics and anxiolytics drugs in recent 2 weeks; no allergy to anesthetic material and no medical history; clinical diagnosis of intact tooth would be confirmed by response to electric pulp tester(PARKELL,PT-20,made in USA) and normal response(short momentary answer). Exclusion criteria:Systemic disease and/or maxillary sinusitis; patients with tooth pain at the time of study; unstable heart disease; allergy to anesthesia material of lidocaine 2% with 1/80000 epinephrine or latex or lidocaine or prilocaine gels; facial or or oral parasthesia; consumption of painkillers,analgesics and anxiolytics drugs in 2 weeks before treatment; presence of periapical radiolucency; pregnancy; breast-feeding; non-repairable tooth and presence of crown

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain intensity. Timepoint: immediately after injection. Method of measurement: visual analoge scale.
Secondary Outcome Measures
NameTimeMethod
Hematoma. Timepoint: 24 hours after treatment. Method of measurement: visual observation(objective).
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