IRCT20240729062577N1RecruitingPhase 3
Evaluation of the effect of lidocaine 2%-dexamethasone composition and compare it with lidocaine 2% injection on postoperative endodontic pain
Shahre-kord University of Medical Sciences0 sites108 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
- Sponsor
- Enrollment
- 108
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 12 years to 60 years (—)
- Sex
- All
Inclusion Criteria
- •Healthy people with ASA I and ASA II
- •The tooth has no history of pulp therapy
- •The state of the pulp is irreversible pulpitis to necrosis
- •Periapical condition of the tooth as acute or chronic periodontitis
- •Not taking painkillers and anti-inflammatory drugs in the last 12 hours
- •Absence of acute or chronic periapical abscess and acute periodontal abscess
- •No need to take prophylactic antibiotics
- •Absence of pregnancy
- •Absence of mental disability
- •Literate to read and write
- •Absence of systemic disease prohibiting root canal treatment
- •Absence of infectious disease or sensitivity to dexamethasone
- •Absence of tooth apex opening
Exclusion Criteria
- •People with ASA III and ASA IV
- •A tooth that requires multiple treatment sessions
- •Age more than 60 and less than 12 years
Investigators
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