MedTrace Logo

The Effect of Different Obturation Techniques on Postobturation Pain in Single-Visit Root Canal Treatment

NCT06146894 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2024-06-06

No results posted yet for this study

Summary

The goal of this prospective clinical randomized study is to evaluate the effect of different obturation techniques on postobturation pain in single-visit root canal treatment in 18-60 years old patient who present no systemic disease (American Society of Anesthesiology class I or II) and require nonsurgical root canal treatment The main question it aims to answer which obturation technique used with bioceramic sealer cause less postobturation pain in single-visit root canal treatment in comparison to AH plus sealer used with lateral condensation or warm vertical compaction.

Participants will receive single visit root canal treatment using bioceramic sealer with different obturation techniques Group 1: Single cone technique Group 2: lateral condensation technique Group 3: Vertical compaction technique to see effect of different obturation technique on postobturation pain in single-visit root canal treatment.

Conditions

  • Postoperative Pain

Interventions

PROCEDURE

Single obturation technique (Bioceramic Sealer)

Root canal will be obturated using single cone technique using Bioceramic Sealer

PROCEDURE

lateral condensation technique (Bioceramic Sealer)

Root canal will be obturated using lateral condensation technique using Bioceramic Sealer

PROCEDURE

Warm Vertical condensation technique (Bioceramic Sealer)

Root canal will be obturated using vertical condensation technique using Bioceramic Sealer

PROCEDURE

lateral condensation technique (AH Plus Sealer)

Root canal will be obturated using lateral condensation technique using AH plus Sealer

PROCEDURE

Warm Vertical condensation technique (AH plus Sealer)

Root canal will be obturated using vertical condensation technique using AH plus Sealer

Sponsors & Collaborators

  • Kafrelsheikh University

    lead OTHER

Principal Investigators

  • Hisham Abada, PhD · Kafrelsheikh University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-12-01
Primary Completion
2024-06-10
Completion
2024-06-28

Countries

  • Egypt

Study Locations

More Related Trials

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 NCT06146894 on ClinicalTrials.gov