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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-12-01

Study Completion Date

2024-06-28

Brief Summary

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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.

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Detailed Description

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Conditions

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Postoperative Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

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Single cone technique (Bioceramic Sealer)

Group Type EXPERIMENTAL

Single obturation technique (Bioceramic Sealer)

Intervention Type PROCEDURE

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

lateral condensation technique (Bioceramic Sealer)

Group Type EXPERIMENTAL

lateral condensation technique (Bioceramic Sealer)

Intervention Type PROCEDURE

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

Warm Vertical condensation technique (Bioceramic Sealer)

Group Type EXPERIMENTAL

Warm Vertical condensation technique (Bioceramic Sealer)

Intervention Type PROCEDURE

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

lateral condensation technique (AH plus Sealer)

Group Type EXPERIMENTAL

lateral condensation technique (AH Plus Sealer)

Intervention Type PROCEDURE

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

Warm Vertical condensation technique (AH plus Sealer)

Group Type EXPERIMENTAL

Warm Vertical condensation technique (AH plus Sealer)

Intervention Type PROCEDURE

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

Interventions

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Single obturation technique (Bioceramic Sealer)

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

Intervention Type PROCEDURE

lateral condensation technique (Bioceramic Sealer)

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

Intervention Type PROCEDURE

Warm Vertical condensation technique (Bioceramic Sealer)

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

Intervention Type PROCEDURE

lateral condensation technique (AH Plus Sealer)

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

Intervention Type PROCEDURE

Warm Vertical condensation technique (AH plus Sealer)

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

Intervention Type PROCEDURE

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes