A clinical trial to study the reduction in inter appointment pain in patient undergoing root canal treatment with different file systems

A Comparative evaluation of reduction in inter-appointment pain in single-rooted teeth with symptomatic irreversible pulpitis using three different NiTi file systems: A randomized clinical study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061936

Enrollment

144

Registered

2024-01-29

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

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

Conditions

None listed

Interventions

Intervention1: rotary files trunatomy: trunatomy rotary files Control Intervention1: edge one files from edge endo: edge one files from edge endo

Eligibility

Inclusion criteria

Inclusion criteria: 1. Systemically healthy Patients (Category: American Society of Anesthesiologists class 1) (ASA House of Delegates 2014) between the age group of 18-60 years with maxillary or mandibular single-rooted (single-canaled) teeth with Symptomatic Irreversible pulpitis with or without symptomatic apical periodontitis will be included in the study. 2. Pre-operative pain categorized as moderate to worst pain, on visual analogue scale (range 4-10) 3. A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Identification of the most effective file system in reduction of inter appointment painTimepoint: baseline , 6 hrs , 12 hrs , 24 hrs , 48 hrs	—

Secondary

Measure	Time frame
improved clinical decision makingTimepoint: baseline , 6hrs , 12 hrs , 24 hrs , 48 hrs	—

Countries

India

Contacts

Public ContactAshwin Surana M

km shah dental college and hospital

drajayinendo@gmail.com8385017307

Outcome results