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

Sponsor

Kafrelsheikh University (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT06146894

Collaborator

(none)

150

Enrollment

Arms

2.9

Anticipated Duration (Months)

Study Details

Study Description

Brief 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

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.

Condition or Disease	Intervention/Treatment	Phase
Postoperative Pain	Procedure: Single obturation technique Procedure: lateral condensation technique Procedure: Vertical condensation technique	N/A

Study Design

Study Type:

Interventional

Anticipated Enrollment :

150 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Single (Participant)

Primary Purpose:

Supportive Care

Official Title:

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

Anticipated Study Start Date :

Dec 1, 2023

Anticipated Primary Completion Date :

Feb 28, 2024

Anticipated Study Completion Date :

Feb 28, 2024

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Single cone technique	Procedure: Single obturation technique Root canal will be obturated using single cone technique
Experimental: lateral condensation technique	Procedure: lateral condensation technique Root canal will be obturated using lateral condensation technique
Experimental: Vertical condensation technique	Procedure: Vertical condensation technique Root canal will be obturated using vertical condensation technique

Arm

Intervention/Treatment

Experimental: Single cone technique

Procedure: Single obturation technique

Root canal will be obturated using single cone technique

Experimental: lateral condensation technique

Procedure: lateral condensation technique

Root canal will be obturated using lateral condensation technique

Experimental: Vertical condensation technique

Procedure: Vertical condensation technique

Root canal will be obturated using vertical condensation technique

Outcome Measures

Primary Outcome Measures

postobturation pain [30 days]
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.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 60 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

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.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

Kafrelsheikh University

Investigators

Principal Investigator: Hisham Abada, PhD, Kafrelsheikh University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Related Info

Publications

None provided.

Responsible Party:

Hisham Mahmoud Hamdy Abada, Doctor, Kafrelsheikh University

ClinicalTrials.gov Identifier:

NCT06146894

Other Study ID Numbers:

HA2427

First Posted:

Nov 27, 2023

Last Update Posted:

Nov 27, 2023

Last Verified:

Nov 1, 2023

Individual Participant Data (IPD) Sharing Statement:

Yes

Plan to Share IPD:

Yes

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Keywords provided by Hisham Mahmoud Hamdy Abada, Doctor, Kafrelsheikh University

Postoperative Pain

Bioceramic sealer

Obturation

Additional relevant MeSH terms:

Pain, Postoperative

Study Results

No Results Posted as of Nov 27, 2023