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Effect of Apical Enlargement to Different Preparation Sizes and Tapers on Pain and Bacterial Reduction in Necrotic Pulp

NCT05620147 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2022-11-21

No results posted yet for this study

Summary

The aim of this prospective randomized clinical trial is to evaluate the effect of different apical size and taper preparation (35. 04; 35. 06; 45. 04 and 45. 06) on postoperative pain at 6, 12, 24, 48 and 72 hours, and intra-canal bacterial count in patients having mandibular premolars with necrotic pulps.

Conditions

  • Necrotic Pulp

Interventions

OTHER

Root canal instrumentation EdgeFile X7 to size #35/0.06

Instrumentation will be performed using an endodontic motor at a speed of 300 rpm and a torque of 2 Ncm

OTHER

Root canal instrumentation EdgeFile X7 to size #45/0.04

Instrumentation will be performed using an endodontic motor at a speed of 300 rpm and a torque of 2 Ncm

OTHER

Root canal instrumentation EdgeFile X7 to size #45/0.06

Instrumentation will be performed using an endodontic motor at a speed of 300 rpm and a torque of 2 Ncm

OTHER

Root canal instrumentation EdgeFile X7 to size #35/0.04

Instrumentation will be performed using an endodontic motor at a speed of 300 rpm and a torque of 2 Ncm

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Nermeen Ibrahim, Master's · Misr University for Science and Technology

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-31
Primary Completion
2023-11-30
Completion
2023-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05620147 on ClinicalTrials.gov