Instrumentation Time Efficiency and Histologically the Debriding Efficacy. (ITE)
Necrosis
About this trial
This is an interventional treatment trial for Necrosis focused on measuring clean, Primary Root canal, rotary instrumentation
Eligibility Criteria
Inclusion Criteria:
- the aims and requirements of the study were freely accepted by the parents
- primary molars with at least 11.0 ± 1.0 mm of working length
- Treatment was limited to patients in good health;
- All teeth had vital and non-vital pulps without a sinus tract;
- Excess of bleeding during a pulpotomy;
- Presence of enough coronal tooth and root structure;
- No prior pulpectomy treatment on the involved tooth,
- absence of perforation in the internal and/or external furcation area and
- No analgesics or antibiotics were used before the clinical procedures began.
Exclusion Criteria:
- patients without inclusion requirements or failure to obtain parent´s authorization, .) patients older than 7 years old,
- had a positive history of antibiotic use within the past month,
- diabetic, hemophilic
- if the tooth had root resorption or been previously accessed and initiated a pulpectomy.
Sites / Locations
- Jorge Paredes Vieyra
- Jorge Paredes Vieyra
- Jose Clemente Orozco
- Jose Clemente
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
Control group
Group 1
Group 2
Control Group (n= 15): the root canals were prepared manually with K-files (Dentsply-Maillefer, Ballaigues, Switzerland) and "step back technique" up to size #35.
Group 1 (n= 15): the root canals were instrumented with rotary LightSpeed LSX instruments (Discus Dental, Culver City, CA, USA). They were used to complete the canal preparation to a size #50 for the anteriors and molar teeth to size #40.
Group 2 (n= 15): root canals were instrumented with ProTaper Next (Dentsply Maillefer, Ballaigues, Switzerland) using X1, X2 to X3. 0.5% NaOCl was used for irrigation.