Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | mepivicane hydrochloride | Pain will be assessed during access cavity preparation and instrumentation |
| DRUG | articane hydrochloride | Pain 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.