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

The Effect of Different Obturation Techniques on Postobturation Pain in Single-Visit Root Canal Treatment: A Prospective Clinical Randomized Study

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.

Study Overview

• Status: Recruiting
• Conditions: Postoperative Pain
• Intervention / Treatment: Procedure: Single obturation technique (Bioceramic Sealer); Procedure: lateral condensation technique (Bioceramic Sealer); Procedure: Warm Vertical condensation technique (Bioceramic Sealer); Procedure: lateral condensation technique (AH Plus Sealer); Procedure: Warm Vertical condensation technique (AH plus Sealer)

• Study Type: Interventional
• Enrollment (Estimated): 150
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Hisham Abada, PhD; Phone Number: 002 01003772427; Email: Hisham.dentist@gmail.com

Study Locations

• Egypt
  • Kafr El-Shaikh
    • Kafr Ash Shaykh, Kafr El-Shaikh, Egypt, 33511
      • Recruiting
      • Kafrelsheikh University
      • Contact: hisham abada, phd

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Patients aged 18-60 years who presented no systemic disease (American Society of Anesthesiology class I or II) and required nonsurgical root canal treatment.
• Diagnosis of asymptomatic irreversible pulpitis in a molar tooth with 3 independent root canals.

Exclusion Criteria:

• Presence of immature root apexes, root fracture, or periodontal disease
• Use of any analgesic, anti- inflammatory, or antibiotics before the treatment.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

5

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Single cone technique (Bioceramic Sealer)	Procedure: Single obturation technique (Bioceramic Sealer); Root canal will be obturated using single cone technique using Bioceramic Sealer
Experimental: lateral condensation technique (Bioceramic Sealer)	Procedure: lateral condensation technique (Bioceramic Sealer); Root canal will be obturated using lateral condensation technique using Bioceramic Sealer
Experimental: Warm Vertical condensation technique (Bioceramic Sealer)	Procedure: Warm Vertical condensation technique (Bioceramic Sealer); Root canal will be obturated using vertical condensation technique using Bioceramic Sealer
Experimental: lateral condensation technique (AH plus Sealer)	Procedure: lateral condensation technique (AH Plus Sealer); Root canal will be obturated using lateral condensation technique using AH plus Sealer
Experimental: Warm Vertical condensation technique (AH plus Sealer)	Procedure: Warm Vertical condensation technique (AH plus Sealer); Root canal will be obturated using vertical condensation technique using AH plus Sealer

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
postobturation pain	Presence of post-obturation pain will accessed by visual analog scale (VAS) scale (0-10), where 0 showed no pain, 1-3 mild pain, 4-6 moderate pain, 7-9 severe pain, and 10 worst possible pain.	30 days

Collaborators and Investigators

• Sponsor: Kafrelsheikh University
• Investigators: Principal Investigator: Hisham Abada, PhD, Kafrelsheikh University

Publications and helpful links

Helpful Links

• Related Info

Study record dates

Study Major Dates

• Study Start (Actual): December 1, 2023
• Primary Completion (Estimated): June 10, 2024
• Study Completion (Estimated): June 28, 2024

Study Registration Dates

• First Submitted: November 17, 2023
• First Submitted That Met QC Criteria: November 24, 2023
• First Posted (Actual): November 27, 2023

Study Record Updates

• Last Update Posted (Actual): June 6, 2024
• Last Update Submitted That Met QC Criteria: June 5, 2024
• Last Verified: June 1, 2024

More Information

Terms related to this study

• Keywords: Postoperative Pain; Bioceramic sealer; Obturation
• Additional Relevant MeSH Terms: Pathologic Processes; Postoperative Complications; Pain; Neurologic Manifestations; Pain, Postoperative
• Other Study ID Numbers: HA2427

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Sharing Supporting Information Type: STUDY_PROTOCOL

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No