Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT07166679

Effect of Apical Third Enlargement to Different Taper and Master Apical Preparation Size on Periapical Healing and Postoperative Pain After Primary Single Sitting Non Surgical Root Canal Treatment

Led by Postgraduate Institute of Dental Sciences Rohtak · Updated on 2025-09-10

270

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To Determine Effect Of Apical Third enlargement To Different Taper And Master Apical Preparation Size On Periapical Healing And Postoperative Pain After Primary Single Sitting Non Surgical Root Canal Treatment : A Randomized Clinical Trial

CONDITIONS

Official Title

Effect of Apical Third Enlargement to Different Taper and Master Apical Preparation Size on Periapical Healing and Postoperative Pain After Primary Single Sitting Non Surgical Root Canal Treatment

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65 years, any gender
  • Asymptomatic teeth with pulpal necrosis and apical periodontitis in a mandibular molar
  • Radiographic evidence of periapical radiolucency with Periapical index (PAI) score of 3 or higher in the mesial root of mandibular molars
Not Eligible

You will not qualify if you...

  • Medically compromised patients
  • Initial apical binding file (IABF) size greater than 20
  • Pregnancy, lactation, or use of contraceptives
  • Antibiotic use within the past month or need for antibiotic premedication for dental treatment including infective endocarditis or prosthetic joint prophylaxis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Pgids Rohtak

Rohtak, India

Actively Recruiting

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Research Team

D

Dr shweta mittal, MDS

CONTACT

D

DR sahil saini, PG STUDENT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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