Health Condition 1: K040- Pulpitis
Conditions
Interventions
Intervention1: TruNatomy Rotary NiTi file system: root canals will be shaped using TruNatomy Rotary NiTi file system
Control Intervention1: TruNatomy Rotary NiTi file system: WaveOne Gold reciprocatin
Sponsors
MGM Dental College and Hospital
Eligibility
Inclusion criteria
Inclusion criteria: 1.All vital single-rooted teeth with irreversible pulpitis, whether associated with or without apical periodontitis, and mild to moderate pain (VAS value 5-74mm) indicated root canal treatment.2.Maxillary and mandibular premolars with single root and single canal.3.Patients with single rooted permanent teeth with periapical radiolucency less than 1.5 mm as determined by an intraoral periapical (IOPA) radiograph. 4.Teeth with fully developed apex and straight canals with minimal curvature (0 to 10 degrees) 5.Teeth with healthy periodontium with periodontal probing depth 3
Exclusion criteria
Exclusion criteria: 1.Pregnant women and lactating mothers. 2. Patients with acute dentoalveolar abscess or cellulitis. 3. Patients presenting with severe pain (75-100mm). 4. Patients who have taken antibiotics and analgesics and corticosteroid in the past month. 5.Patients with known immunocompromised conditions (e.g., AIDS) 6.Patients who are known diabetic. 7.Patients with non-vital teeth and intraoral and extraoral sinus tract 8.Patients with radiographic evidence of radiolucency of more than 1.5 mm 9. Patients who are having teeth with Single roots having multiple canals, bifurcation and trifurcation of canals, canal aberration, calcified canals. open apex, root resorption. presence of root caries and multirooted teeth 10. Teeth with aggressive periodontitis and grade III mobility, periodontal probing depth >3mm.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| compare the of post-operative pain in single-visit endodontics where canal instrumentation will be done using two different rotary instrument systems. For each patient, the preoperative and post-operative pain levels will be recorded by using a visual analogue scale (VAS)Timepoint: The assessment of the post-operative pain will be conducted at intervals of 6 hours, 24 hours, and 7 days after the initial visit. | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Public ContactDr Anuradha Patil
MGM DENTAL COLLEGE AND HOSPITAL, KAMOTHE
Outcome results
None listed