Skip to content

the success of inferior alveolar nerve block with intraligament or buccal infiltration in mandibular posterior teeth

Comparison the success of inferior alveolar nerve block with intraligament or buccal infiltration in mandibular first molar with symptomatic irriversible pulpitis : A randomized control clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20101108005141N6
Enrollment
96
Registered
2018-02-03
Start date
2018-01-09
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

pulp disease. Diseases of pulp and periapical tissues

Interventions

Intervention 1: Control group: In the control group, standard block injection was performed using Articanin 4% solution (Artinibsa
Inibsa, Barcelona, Spain) with epinephrine 100000/1. After 15 minutes, the anesthetized teeth were isolated and the cavity was prepared and access prepration will be done. Intervention 2: Intervention
Inibsa, Barcelona, Spain) with an epinephrine of 100,000/1. After 15 minutes of block anesthesia and numbness of the lips, an infiltration on the buccal side of the affected tooth will be performed at

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Systemically healthy patient Subjects 18-65 years of age No sensivity to epinephrin and articaine No facial parastacidae Do not use any medication 6 hours before treatment Not taking any medication that interferes with numbness No pathoes in the areas of injection Patient not to be pregnant Absence of pathologic pockets during probing The patient with the first molar with symptomatic irriversible pulpitis

Exclusion criteria

Exclusion criteria: Any illness that is unable to fill the informed consent form history of trauma

Design outcomes

Primary

MeasureTime frame
The amount of pain. Timepoint: during access cavity preparation and entrance in to the pulp chamber and the root canal. Method of measurement: Use Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr shahriar shahi

Periodontal and dental research center

sshahriar32@gmail.com+98 41 3335 5965

Outcome results

None listed

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