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The Incidence of Postoperative Pain After Using Different Types of Sealers

B

British University In Egypt

Status

Enrolling

Conditions

Resin Based Sealers
Root Canal Sealers
Sillicon Based Sealers
Post Operative Pain

Treatments

Procedure: Glide path
Diagnostic Test: Visual Analogue Scale (VAS)
Drug: application of resin based sealer inside the canal in the resin based sealer group
Procedure: Working Length Determination (W.L)
Procedure: Master cone check
Procedure: Obturation
Procedure: Irrigation
Procedure: Supplemental local anesthesia
Procedure: Primary local anesthesia
Procedure: Canal negotiation
Procedure: Activation of the irrigant
Diagnostic Test: application of the sillicon based sealer inside the canal in the sillicon based group
Procedure: Apical gauging
Procedure: Second w.l determination
Procedure: Cleaning and shaping using rotary system
Procedure: Coronal flaring
Procedure: Removal Of Caries and Access Cavity
Procedure: Bleeding control
Procedure: Rubber dam isolation of tooth

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this randomized clinical trial is to evaluate and compare the incidence and intensity of post-operative pain after obturation using resin and silicon-based sealers.

Full description

The main objectives of root canal therapy are to achieve long-term comfort, function, and aesthetics for the patients and prevention of reinfection of tooth. These objectives are provided through complete cleaning, shaping, and obturation of canals of affected teeth .

Some patients may report moderate-to-severe pain and/or swelling following root canal treatment .

This is detrimental for both patient and dentist and may entail an unscheduled emergency visit by patients to relieve their symptoms.

Postoperative pain is considered a clinical outcome that exhibits the multifactorial nature of patients' responses to variables among treatment procedures such as maintaining the working length to the apical constriction, finishing the endodontic treatment in single visit or multiple visit, instrumentation technique and the type of endodontic sealer used for obturation .

Such pain occurrence is mainly due to mechanical, chemical or microbial injury to the periapical tissues .

Trauma of periapical tissue or bacterial extrusion and root canal sealer specifically, extrusion of root canal sealer can disrupt periodontal tissues and cause inflammatory reactions. The intensity of this reaction depends on the composition of the sealer .

Root canal sealers can play a crucial role in this regard by coming in contact with the periapical tissues through apical foramen and lateral canals causing a localized inflammation with a direct influence on the degree of inflammation based on the composition of the sealer in turn influencing postoperative pain levels .

Silicone is inert and biocompatible and has been widely used in medicine as an implant material Silicone-based root-canal sealers are also available. However, there are no data on the clinical performance of this type of material in endodontic treatment .

Enrollment

50 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • • Patient's age ranges from 18-50 years old.

    • Patients with teeth diagnosed with symptomatic irreversible pulpitis.
    • Normal periapical condition confirmed by normal periapical radiograph
    • The teeth are restorable
    • Teeth are periodontally free, with no mobility and negative to percussion and palpation test.

Exclusion criteria

  • • Teeth with immature roots

    • Non restorable teeth
    • Medically compromised patients with systemic complication that would alter the treatment.
    • Necrotic teeth
    • Teeth with apical periodontitis or periapical lesions
    • necrotic Teeth.

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

Group (1) Resin Based Sealer intervention
Experimental group
Description:
evaluate the incidence and intensity of post-operative pain after obturation using resin based sealers.
Treatment:
Procedure: Rubber dam isolation of tooth
Procedure: Bleeding control
Procedure: Removal Of Caries and Access Cavity
Procedure: Coronal flaring
Procedure: Cleaning and shaping using rotary system
Procedure: Apical gauging
Procedure: Second w.l determination
Diagnostic Test: application of the sillicon based sealer inside the canal in the sillicon based group
Procedure: Activation of the irrigant
Procedure: Canal negotiation
Procedure: Primary local anesthesia
Procedure: Supplemental local anesthesia
Procedure: Obturation
Procedure: Irrigation
Procedure: Master cone check
Procedure: Working Length Determination (W.L)
Diagnostic Test: Visual Analogue Scale (VAS)
Drug: application of resin based sealer inside the canal in the resin based sealer group
Procedure: Glide path
Group (2) Silicone Based Sealer intervention
Experimental group
Description:
evaluate the incidence and intensity of post-operative pain after obturation using sillicon based sealers.
Treatment:
Procedure: Rubber dam isolation of tooth
Procedure: Bleeding control
Procedure: Removal Of Caries and Access Cavity
Procedure: Coronal flaring
Procedure: Cleaning and shaping using rotary system
Procedure: Apical gauging
Procedure: Second w.l determination
Diagnostic Test: application of the sillicon based sealer inside the canal in the sillicon based group
Procedure: Activation of the irrigant
Procedure: Canal negotiation
Procedure: Primary local anesthesia
Procedure: Supplemental local anesthesia
Procedure: Obturation
Procedure: Irrigation
Procedure: Master cone check
Procedure: Working Length Determination (W.L)
Diagnostic Test: Visual Analogue Scale (VAS)
Drug: application of resin based sealer inside the canal in the resin based sealer group
Procedure: Glide path

Trial contacts and locations

1

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Central trial contact

Kareem Mohammed Elhoseny, ORCID:0009-0001-6101-5615, Bachelor; Engy Medhat Kataia, professor at BUE

Data sourced from clinicaltrials.gov

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