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Comparison of Pain After Root Canal Treatment With and Without Coronal Preflaring in Lower Premolar Teeth Using Two Different File Systems

Comparison Of Post-Operative Pain After Root Canal Treatment With And Without Coronal Preflaring In Mandibular Premolars With Symptomatic Irreversible Pulpitis Using Two Different File Systems: A Randomised Clinical Trial. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108765
Enrollment
136
Registered
2026-04-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Root canal treatment using coronal preflaring instruments with HyFlex EDM and NeoEndo S NiTi rotary files.: Root canal treatment will be performed using HyFlex EDM and NeoEndo S NiTi ro
followed by standardized procedures including access preparation. working length determination, glide path preparation, cleaning and shaping, irrigation, obturation, and restoration. The procedure wil

Sponsors

JN Kapoor D A V C Dental College Room No Model Town Yamunanagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with symptomatic irreversible pulpitis without tenderness on percussion in mandibular premolar teeth. 2. Teeth where number 10 K files can reach and fit the Working length. 3. Patients who are able to understand the informed consent form and pain recording scales used in the study

Exclusion criteria

Exclusion criteria: 1. Teeth that are difficult to isolate with rubber dam. 2. Teeth with no occlusal contact. 3. Previously initiated root canal treatment. 4. Teeth with calcified root canaL. 5. Teeth with internal/external root resorption 6. Teeth with multiple root canals. 7. Teeth with crown and/or root fracture. 8. Patients who received analgesics or anti-inflammatory drugs in the last 72 hours and antibiotics for the last 1 week.

Design outcomes

Primary

MeasureTime frame
1. pain 2. analgesic intake 3. periapical extrusionTimepoint: 1.pain - at baseline, 6hrs, 24hrs, 48hrs, 72hrs, 1 week 2. analgesic intake- 6hrs, 24hrs, 48hrs, 72hrs, 1 week 3.periapical extrusion-present or absent after obturation.

Secondary

MeasureTime frame
Instrument fractureTimepoint: during the procedure

Countries

India

Contacts

Public ContactDr Poonam Bogra

D. A. V. (c) dental college, yamunanagar

poonambogra@yahoo.in9050462962

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026