Irreversible Pulpitis. Pulpitis
Conditions
Interventions
Intervention 1: in Formocresol group , Following the removal of caries and exposure of the pulp, the coronal pulp tissue was removed.A sterile cotton pellet soaked in sterile saline, after cotton pell
Treatment - Drugs
in Formocresol group , Following the removal of caries and exposure of the pulp, the coronal pulp tissue was removed.A sterile cotton pellet soaked in sterile saline, after cotton pellet soaked in for
in 3Mixtatin group, Following the removal of caries and exposure of the pulp, the coronal pulp tissue was removed.A sterile cotton pellet soaked in sterile saline. The cotton pellet was removed from t
in Mineral trioxide aggregate group (MTA), Following the removal of caries and exposure of the pulp, the coronal pulp tissue was removed.A sterile cotton pellet soaked in sterile saline. The cotton pe
Sponsors
Tabriz Faculty of Dentistry
Eligibility
Sex/Gender
All
Age
3 Years to 6 Years
Inclusion criteria
Inclusion criteria: Procedure, possible risks, as well as possible benefits will be thoroughly explained to the parents of the patients aged 3-6 years old and a written informed consent will be taken. Teeth have to had appropriate clinical and radiographic sign and symptoms: 1. Caries primary molars with vital pulp 2. No history of spontaneous 3. No swelling (of pulpal origin) 4. No fistula 5. No pathological tooth mobility 6. No pathologic external root resorption 7. No pathological internal root resorption 8. No periapical or interradicular radiolucency 9. No pulp calcifications 10. No excessive bleeding from the amputated radicular stumps. 11. No history of nocturnal pain 12. No tenderness to percussion or palpation 13. Normal gingival and periodontal condition 14. Absence of periapical or furcal radiolucencies 15. Complete physical and mental health 16. Available to be restored by amalgam or SSC 17. Availability for 3 months follow up
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dental hard tissue formation. Timepoint: Before and 3 months after intervention. Method of measurement: Radiography. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Before and 3 months after intervention. Method of measurement: Question and palpation.;Mobility. Timepoint: Before and 3 months after intervention. Method of measurement: Palpation.;Bone radiographic repair. Timepoint: Before and 3 months after intervention. Method of measurement: Radiography. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Vajihe Alavi
Tabriz Faculty of Dentistry
Outcome results
None listed