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Comparative evaluation of the effects of conventional and computer-aided anesthesia methods on pain and anxiety in pediatric patients with molar incisor hypomineralization

Comparative evaluation of the effects of conventional and computer-aided anesthesia methods on pain and anxiety in pediatric patients with molar incisor hypomineralization

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20241120001
Enrollment
66
Registered
2024-11-20
Start date
2024-11-25
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Comparative evaluation of the effects of different anesthesia techniques on the patients&#039

Interventions

Mandibular anesthesia by traditional injection method,Mandibular anesthesia with computer-aided digital anesthesia method,Intraosseous anesthesia with computer-aided digital anesthesia method
Traditional injection anesthesia,Computer-aided digital anesthesia,Computer-aided digital anesthesia

Sponsors

Mersin University Scientific Research Projects Unit
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1) Having molar incisor hypomineralization, no comprehension or speech problems and being willing to participate in the study, 2) The legal representative's child being willing to participate in the study and his/her consent being obtained, 3) Not having a systemic disease that would constitute a contraindication for dental treatment or anesthesia and not using regular medication, 4) The patient group not having any physical or physical disabilities, 5) Not having any hereditary or acquired diseases or syndromic conditions, 6) Not having had any previous dental treatment, 7) Having active caries that did not exceed 1/3 of the dentin in the mandibular right or left first molar teeth, 8) Teeth requiring Class II cavity preparation, 9) Not having a history of acute pain

Exclusion criteria

Exclusion criteria: 1) Children with no molar hypomineralization, who do not volunteer to participate in the study, who have the potential to harm others, who cannot do their own work, understand, make decisions, speak due to mental weakness, or who require constant assistance for their protection and care, 2) Children whose legal representatives do not volunteer for their children to participate in the study and whose consent cannot be obtained, 3) Children who do not sign the informed consent form and their legal representatives, 4) Patients with systemic diseases and regular medication use, 5) Patients with irreversible pulpitis, cellulitis findings and acute pain, 6) Teeth with caries exceeding 1/3 of the dentin, teeth with indications for amputation and root canal treatment, 7) Syndromic individuals with hereditary and acquired diseases, 8) Those who have previously had any trauma to their teeth to be treated, 9) Patients who report an allergy to local anesthetic drugs, 10) Patients in the definitely negative group according to the Frankl behavior scale

Design outcomes

Primary

MeasureTime frame
Pain Before and after anesthesia Scale and salivary opiorphin value

Secondary

MeasureTime frame
Anxiety Before and after anesthesia Scale and salivary opiorphin value

Countries

Turkey

Contacts

Public ContactMeryem Sahin

Faculty of Dentistry, Mersin University

meryem.sahin@mersin.edu.tr903243610101

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026