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The effect of tactile or visual determination of injection site on subjective and objective pain reactions and success rate of inferior alveolar nerve block in children

The effect of tactile or visual determination of injection site on subjective and objective pain reactions and success rate of inferior alveolar nerve block in children

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201605116105N5
Enrollment
40
Registered
2016-06-02
Start date
2016-09-09
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

Local anesthesia,. Local anaesthetics

Interventions

Intervention 1: Intervention 1: Applying topical anesthesia gel (TOPEX, Sultan Healthcare IND. CO, USA) by cotton applicator at the injection site on dried mucosa for 60 seconds, administration mandi
Treatment - Other
Intervention 1: Applying topical anesthesia gel (TOPEX, Sultan Healthcare IND. CO, USA) by cotton applicator at the injection site on dried mucosa for 60 seconds, administration mandibular block ane
Intervention 2: Applying topical anesthesia gel (TOPEX, Sultan Healthcare IND. CO, USA) by cotton applicator at the injection site on dried mucosa for 60 seconds, administration mandibular block anes

Sponsors

Vice chancellor for Research, Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 9 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: children between 7-9 years old, require treatment in the mandibular second primary molar, a full physical and mental health, located in the classification of Frankel positive or definitely positive during behavioral assessment before treatment, identified the pterygomandibular triangle landmark in intraoral examination. Exclusion criteria: previous dental history, allergies to medication or anesthetic, emergency mode or pulp origin tooth pain, no need to premedication before dental treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Objective and subjective pain reaction. Timepoint: During injection and after intervention 1 and 2. Method of measurement: Using SEM scale and using FIS.

Secondary

MeasureTime frame
Success of anesthesia. Timepoint: During access cavity preparation, after intervention 1 and 2 and 5 minutes waiting period. Method of measurement: Using SEM scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNahid Ramazani

Zahedan dentistry School

ramazani_nahid@yahoo.com+98 54 3342 3218

Outcome results

None listed

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