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Outcome Following Endodontic Treatment Using Traditional Access Versus Conservative Access

Pulpitis - Irreversible Clinical Trial

Official title:
Comparative Evaluation of Outcome Following Endodontic Treatment Using Traditional Versus Conservative Access in Mandibular Molars With Symptomatic Irreversible Pulpitis: a Randomized Controlled Trial

Clinical Trial Summary

This study will compare the outcome of endodontic treatment using conservative or traditional access design in permanent molars with clinical signs indicative of irreversible pulpitis

Clinical Trial Description

After thorough history and clinical and radio graphic examination, and confirmation of eligibility for the study, written informed consent will be obtained after explaining the procedure and its associated risks and benefits. Clinical diagnosis of symptomatic irreversible pulpitis will be established based on a history of spontaneous pain or pain exacerbated by cold stimuli and lasting for a few seconds to several hours (lingering pain) compared to control teeth and which is reproducible using cold testing. Once included, study subjects will be randomly allocated to either traditional access or conservative access group. Subsequently biomechanical preparation will be carried out using standard protocol with the use of rotary NiTi file system followed by root canal filling using gutta percha and zinc oxide eugenol sealer. Teeth will be restored using composite resin in the same appointment. Pain analysis will be carried out preoperatively and postoperatively at every 24 hours till 7 days after intervention. All the subjects will be followed up for evaluation of success at 6 and 12 months from baseline. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05402098
Study type Interventional
Source Postgraduate Institute of Dental Sciences Rohtak
Contact DR. ANKITA RAMANI, MDS
Phone +919582841539
Email ramaniankita95@gmail.com
Status Recruiting
Phase N/A
Start date May 12, 2022
Completion date September 2023
View Details
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