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About
this prospective in vivo randomized clinical is to evaluate the post operative pain (incidence ,degree and duration) with multiple full rotation file (protaper next ®) and single full rotation file (Neolix®) in treating maxillary and mandibular anterior and premolar with chronic pulpitis .Together with our aim from this trial ; we are trying to provide an evidence for the dentists in order to provide the best quality service with the least expenses and thus gaining the patients' trust and saving time, money and effort.
Full description
Interventions:
Using neolix file (Ori kam SAS,France)
Control:
Using Protaper next files (Dentsply ,Maillefer , Switzerland)
Treatment in all cases will be completed in one session as follows:
Full medical and dental history using a schematic dental chart will be obtained from all patients treated during this study. Each tooth will be evaluated for vitality (sensitivity) of pulp tissues using electric pulp tester (Kerr, Analytic Technology Crop, Redmond, WA).
Patient will be anesthetized; teeth will be isolated with rubber dam.
Make access and working length will be determined using an electronic apex locator (Root ZX, J.Morita USA, Irvine, CA.) then confirmed with intraoral periapical radiograph, to be 0.5-1 mm, shorter than radiographic apex.
Cleaning and shaping will be done using crown down preparation technique with rotary files either
The rotary files will be introduced inside the canal using EDTA gel "MD-Chelcream, META BIOMED CO.,LTD, Korea".
The canals will be thoroughly irrigated using 3 ml of 2.5% Sodium hypochlorite between every subsequent instrument. After instrumentation of the canals, paper points will be used for drying.
Obturation will be carried out using gutta percha cones (25/0.6 or 40/0.4) Or Protaper next cones according to instrument used and canal size with resin sealer (ADSEAL, META BIOMED CO., LTD,Korea).After obturation a cotton pellet will be placed in the pulp chamber and the access cavity will be closed with a temporary filling to avoid coronal leakage. ((MD-Temp, META BIOMED CO., LTD, Korea).
The patient is given a Numerical Rating Scale and asked to rate his pain level at 6, 12, 24 & 48 hours after obturation.
Enrollment
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Inclusion criteria
Exclusion criteria
• Pregnancy or lactation.
Primary purpose
Allocation
Interventional model
Masking
50 participants in 1 patient group
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Central trial contact
siza yacoub el zakhary, professor; karim ahmed nahas, master degree candidate
Data sourced from clinicaltrials.gov
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