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Anesthetic Efficacy of Gow-Gates Nerve Block, Inferior Alveolar Nerve Block, and Their Combination in Mandibular Molars in Patient with Symptomatic Irreversible Pulpitis

Anesthetic Efficacy of Gow-Gates Nerve Block, Inferior Alveolar Nerve Block, and Their Combination in Mandibular Molars in Patient with Symptomatic Irreversible Pulpitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201705092541N5
Enrollment
150
Registered
2017-07-10
Start date
2017-02-19
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

irriversible pulpitis. Pulpitis: NOS acute chronic (hyperplastic)(ulcerative) irreversible reversible

Interventions

Intervention 1: The patients received two GGNB injections of 1.8 mL 2% lidocaine with 1:180,000 epinephrine. Intervention 2: The patients received two IANB injections of 1.8 mL 2% lidocaine with 1:80,
Treatment - Other
The patients received two GGNB injections of 1.8 mL 2% lidocaine with 1:180,000 epinephrine
The patients received two IANB injections of 1.8 mL 2% lidocaine with 1:80,000 epinephrine
The patients received one GGNB injection plus one IANB injection of 1.8 mL 2% lidocaine with 1:80,000 epinephrine

Sponsors

Vice chancellor for research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Eighteen years of age and over; being in good health condition; having a mandibular first molar tooth with symptomatic irreversible pulpitis; not having severe periodontal problem; normal periapical radiographic appearance (other than a widened periodontal ligament); no history of allergy to local anesthesia or sulfite Exclusion criteria: pregnancy; lactation; taking any medications that might influence anesthetic assessment; swelling or having fistula near target tooth; active sites of pathosis in area of injection; any problem that patient could not give informed consent; lack of lip numbness within 15 minutes after injection

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Initial pain. Timepoint: Before treatment. Method of measurement: Heft-Parker Visual Analog Scale (VAS).

Secondary

MeasureTime frame
Post pain. Timepoint: During procedure. Method of measurement: Heft-Parker Visual Analog Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoud Saatchi

Isfahan University of Medical Sciences

saatchi@dnt.mui.ac.ir+98 31 3792 2822

Outcome results

None listed

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