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Comparing of the efficay of Articaine and Lidocaine on Anesthesia of Maxillary first Molars in 4-6years old children

Comparison of anesthetic ef?cacy of 4% articaine and 2% lidocaine for maxillary primary molar buccal in?ltration during routine dental treatment in 4-6years old children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017101036699N1
Enrollment
74
Registered
2017-11-13
Start date
2017-11-22
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.

Interventions

Intervention 1: In group 1, an infiltration with articaine 4% with epinephrine 1 /100,000 will be informed as following.The syringe is parallel to the longitudinal axis of the tooth at the depth of th
Treatment - Drugs
In group 1, an infiltration with articaine 4% with epinephrine 1 /100,000 will be informed as following.The syringe is parallel to the longitudinal axis of the tooth at the depth of the buccal mucosa
In group2, an infiltration of lidocaine 2% with epinephrine of 1/1: 80000 will be informed as following. The syringe is parallel to the longitudinal axis of the tooth at the depth of the buccal muco

Sponsors

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

Eligibility

Sex/Gender
All
Age
4 Years to 6 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Children aged 4-6 years old; Children who are 3 or 4 in Frankel's terms of cooperation; Children with primary maxillary first molar teeth need pulpotomy treatment and confirmed radiographic symptoms require pulpal therapy; Children who have no inflammatory lesions (abscess, fistula) in their buccal mucosa; Children who do not desire spontaneous pain or nighttime pain in their teeth; Exclusion criteria: Children who are 1 or 2 in Frankel's terms of cooperation; Children who need to surface restoration of the primary first molar; Children who require tooth extraction of the primary first molar; Children who have inflammatory lesions in their buccal mucosa; Tooth necrosis; Children who have spontaneous pain or nighttime pain in their teeth; Children who have hyperemic pulp after exposation of their teeth; Radiography of irreversible pulpitis symptoms such as internal resorbtion, external resorbtion, PDL dilatation, radiolucency in furca.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anesthesia of the maxillary primary first molar. Timepoint: 5 minutes after intervention and during work. Method of measurement: By observing the child's behavior with SEM(Sound-Eye-Motor) scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Pourkazemi

Tabriz University of Medical Sciences

pourkazemim@tbzmed.ac.ir00

Outcome results

None listed

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