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UnknownNCT03725579

Anesthetic Efficacy of 2% Mepivacaine Versus 4% Articaine

Anesthetic Efficacy of 2% Mepivacaine Versus 4% Articaine for Inferior Alveolar Nerve Blocks in Patients With Symptomatic Irreversible Pulpitis in Mandibular Molars: A Randomized Clinical Trial PART 6

Status
Unknown
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
66 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
20 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The aim of this prospective randomized clinical trial was compare between 2% Mepivacaine and 4% Articaine for inferior alveolar nerve blocks in patients with symptomatic irreversible pulpitis in mandibular molars as regards to their anesthetic efficiency; during access cavity preparation and instrumentation.

Detailed description

Sixty-six patients diagnosed clinically and radiographically with symptomatic irreversible pulpitis in mandibular posterior teeth will received single-visit root canal treatment using ProTaper Universal rotary system for canal preparation, then they will be randomly divided into two groups (n=33) according to the anesthetic solution used, either Group M (3.6 ml Mepivacaine hydrochloride 2% with 1:100000 epinephrine) or Group A (3.4 ml Articaine hydrochloride 4% with 1:100000 epinephrine). The pain will be assessed using numerical rating scale (NRS) during access cavity preparation and instrumentation, then the need for supplemental anesthesia will be also recorded.

Conditions

Interventions

TypeNameDescription
DRUGmepivicane hydrochloridePain will be assessed during access cavity preparation and instrumentation
DRUGarticane hydrochloridePain will be assessed during access cavity preparation and instrumentation

Timeline

Start date
2018-09-15
Primary completion
2018-12-01
Completion
2018-12-01
First posted
2018-10-31
Last updated
2018-11-01

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03725579. Inclusion in this directory is not an endorsement.