About this trial
The goal of this randomized clinical trial is to evaluate pain after root canal treatment using two different kinds of sealers during obturation in 60 healthy , male and female patients ages between 18 to 40 years. The main aims is to systematically evaluate and compare post-operative pain levels in patients undergoing root canal treatment with two different types of endodontic sealers: AH plus (SEAL APEX) and bio ceramic sealer(META)
• By identifying the sealer that leads to the least discomfort, this research could significantly enhance patient care, minimize recovery time, and improve overall treatment success in endodontics.
Participants in both groups will be given a visual analogue scale(VAS) to measure the pain level after the root canal treatment has been completed. They will measure pain levels at 12, 24 and 48 hours. All information will be recorded on proforma and compared.
Eligibility criteria
Qualifiers
• Patients ranging from 18 to 40 years.
Patients whose teeth have been diagnosed with Symptomatic irreversible pulpitis.
maxillary and mandibular teeth.
A normal periapical condition on radiograph, or one with little to no periodontal ligament (PDL) space widening, confirming the normal periapical state.
Disqualifiers
Non-restorable teeth.
Patients with poor health whose systemic complications could change the course of treatment.
Teeth with immature roots.
Teeth with periapical lesions or apical periodontitis.
Trial design
Treatments tested in this trial
- AH-Plus Epoxy Resin Sealer
- bioceramic sealer
Treatment groups
Sponsors and collaborators
Jaweria Gul Keyani
Lead sponsor
Margalla Institute of Health Sciences
Sponsor institution