The Incidence of Postoperative Pain After Using Different Types of Sealers
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-50
SponsorBritish University In Egypt
About this trial
The aim of this randomized clinical trial is to evaluate and compare the incidence and intensity of post-operative pain after obturation using resin and silicon-based sealers.
Eligibility criteria
Qualifiers
• Patient's age ranges from 18-50 years old.
Patients with teeth diagnosed with symptomatic irreversible pulpitis.
Normal periapical condition confirmed by normal periapical radiograph
The teeth are restorable
Disqualifiers
• Teeth with immature roots
Non restorable teeth
Medically compromised patients with systemic complication that would alter the treatment.
Necrotic teeth
Trial design
Treatments tested in this trial
- Primary local anesthesia
- Supplemental local anesthesia
- Removal Of Caries and Access Cavity
- Rubber dam isolation of tooth
- Bleeding control
- Canal negotiation
- Coronal flaring
- Working Length Determination (W.L)
- Glide path
- Irrigation
- Cleaning and shaping using rotary system
- Second w.l determination
- Apical gauging
- Activation of the irrigant
- Master cone check
- application of resin based sealer inside the canal in the resin based sealer group
- application of the sillicon based sealer inside the canal in the sillicon based group
- Obturation
- Visual Analogue Scale (VAS)
Treatment groups
50 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov