maxiÅŸÅŸary primary molar teeth requiring pulpectomy needle,
Conditions
Interventions
each canal was irrigated with 5 mL 1% NaOCl using a syringe and a 30-
gauge double side-
vented needle (NaviTip
UT) placed 1 mm short of the WL during the root canal preparation.,each canal was irrigated with 5 mL 1% sodium hypochlorite (NaOCl) using a syringe and a 30-
gauge open-
ended needle placed 2 mm short of the WL during the root canal preparation.
Experimental Other,Experimental Other
side-
vented needle group,open-
ended needle group
Sponsors
no
Eligibility
Sex/Gender
All
Age
6 Years to 9 Years
Inclusion criteria
Inclusion criteria: - Upper primary molar teeth requiring pulpectomy - Patients with no history of taking analgesics and antibiotic 12 hours before the pulpectomy - Cooperative patients in ages ranging from 6 to 9 years - Absence of internal or external pathologic root resorption - Presence of adequate coronal tooth structure - Two-thirds of each root remaining - Parent or guardian agree for participant to take part in the study
Exclusion criteria
Exclusion criteria: - Excessive mobility (greater than grade 1 mobility) - Children with underlying systemic disease - Children with special health care needs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain 1 week VAS | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative percussion pain 1 week VAS | — |
Countries
Turkey
Contacts
Public ContactGamze Topcuoglu
Erciyes University
Outcome results
None listed