pulpal inflammation young permanent teeht, presepsin, IL-6,IL-8,TNF-a, IL-1B
Conditions
Interventions
The reversible pulpitis group included teeth in which the pain was not spontaneous or only provoking pain due to hot and cold or food pressure, there was no sensitivity to suction and palpation, pulpa
Diagnostic,Diagnostic
reversible pulpitis,irreversible pulpitis
Sponsors
Coordinatorship of Scientific Research Projects
Eligibility
Sex/Gender
All
Age
6 Years to 12 Years
Inclusion criteria
Inclusion criteria: Systemically healthy children aged 6-12 years, Teeth with a carious lesion that has reached or is very close to the pulp in the 1st or 2nd permanent molars whose root end is not closed, Teeth that can be restored, Swelling, redness or fistula in the vestibular sulcus, pathological mobility, etc. teeth without pathological findings, Teeth in which no lesion is seen radiographically in the furcal or periapical area, but enlargement of the periodontal ligament can be seen in the periapical area that can be diagnosed as acuteapical periodontitis, Teeth in which pathologies such as internal or external resorption are not detected radiographically, During the treatment; bleeding is not too severe and bleeding under 5 minutes The study will be carried out on the teeth that can be stopped.
Exclusion criteria
Exclusion criteria: Children with systemic diseases, Teeth that have completed root development, In children with irreparable loss of material and with tooth germ number 8 on the radiograph, in cases where there is a high probability of closure of the cavity by showing a bodily shift of teeth 7 and 8 into the extraction cavity, Clinically; teeth with advanced pathological conditions such as swelling, abscess, mobility, fistula, Radiographically significant lesion in the furcation or periapical area, Teeth with radiographic evidence of internal or external resorption, Teeth in which bleeding was very severe during treatment and could not be stopped in less than 5 minutes were excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| biomarker amount measurement using ELISA kit 3m ng/ml | — |
Secondary
| Measure | Time frame |
|---|---|
| clinical evaluation of pulpal inflammation 3m presence of pain, pulp haemorrhage longer than 3-5 minutes, dark and severe, | — |
Countries
Turkey
Contacts
Public ContactAybike BAS
Ataturk University
Outcome results
None listed