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Comparison of anesthetic efficacy of articaine in different anesthetic administration methods in the lower jaw molars

Comparative evaluation of anesthetic efficacy of inferior alveolar nerve block plus buccal or lingual infiltration with articaine in painful mandibular molars with irreversible pulpitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014120820238N1
Enrollment
60
Registered
2015-02-21
Start date
2014-12-30
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Irreversible Pulpitis. Pulpitis

Interventions

Intervention 1: Local Anesthesia administration in mandible with Articaine 4% with 1:100000 Epinephrine ,3.6 ml Group 1 : Inferior Alveolar nerve Block Anesthesia For First Molar. Intervention 2: Loca
Treatment - Other
Local Anesthesia administration in mandible with Articaine 4% with 1:100000 Epinephrine ,3.6 ml Group 3 : Inferior Alveolar nerve Block anesthesia with Lingual infiltration for First Molar
Local Anesthesia administration in mandible with Articaine 4% with 1:100000 Epinephrine ,3.6 ml Group 4 : Inferior Alveolar nerve Block Anesthesia For Second Molar
Local Anesthesia administration in mandible with Articaine 4% with 1:100000 Epinephrine ,3.6 ml Group 5 : Inferior Alveolar nerve Block Anesthesia plus Buccal infiltration for Second molar
Local Anesthesia administration in mandible with Articaine 4% with 1:100000 Epinephrine ,3.6 ml Group 1 : Inferior Alveolar nerve Block Anesthesia For First Molar
Local Anesthesia administration in mandible with Articaine 4% with 1:100000 Epinephrine ,3.6 ml Group 2 : Inferior Alveolar nerve Block Anesthesia plus Buccal infiltration for First molar
Local Anesthesia administration in mandible with Articaine 4% with 1:100000 Epinephrine ,3.6 ml Group 6 : Inferior Alveolar nerve Block anesthesia plus Lingual infiltration for Second Molar

Sponsors

Tehran University of Medical Sciences International Campus Dentistry School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Exclusion criteria: Patients with systemic Diseases , Patients that have used any form of sedatives in the past 12 hours , Patients that have allergies to anesthetics or sulfites, Pregnancy , Patients that are unable to give Informed Consent , Patients with Periapical Lesions. Inclusion criteria :Patients between the ages of 18 to 60 , Patients with first and second mandibular molars diagnosed with Symptomatic Irreversible Pulpitis

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: after 20 minutes. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAdel Ardestani

Tehran University of Medical Sciences International Campus Dentistry School

ardestani.adel@gmail.com+98 21 5585 1149

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026