Effect of Sonic Activation of Irrigant on Post Operative Pain After Root Canal Treatment

NCT ID: NCT07062419

Last Updated: 2025-10-01

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

COMPLETED

Clinical Phase

NA

Total Enrollment

58 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-01-01

Study Completion Date

2025-08-30

Brief Summary

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Fifty-eight patients aged 18-60 years, diagnosed with symptomatic or asymptomatic apical periodontitis will be randomly allocated into two groups: Group A (EndoActivator) and Group B (conventional syringe irrigation). preoperative pain will be evaluated in all patients requiring root canal treatment using visual analogue scale before initiating the procedure.

Postoperative pain will be measured using the Visual Analog Scale (VAS) at 24, 36, 48 hours and one week.

Detailed Description

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This randomized clinical study will evaluate the effect of two different irrigation techniques on postoperative pain following root canal treatment in patients with apical periodontitis. A total of 58 patients will be randomly assigned to one of two groups: one group will receive irrigation using the EndoActivator system, while the other group undergo conventional syringe irrigation. The objective is to determine whether the irrigation technique influences the level of postoperative discomfort experienced by patients. Pain levels will be assessed at specific time intervals to track the pattern of recovery and provide insight into the clinical effectiveness of each method in terms of patient comfort.

Conditions

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Post Operative Pain Root Canal Therapy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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one group will receive irrigation during root canal treatment will be activated by an Endoactivator

activation of an irrigant by using certain ultrasonic frequency to enhance antimicrobial action of irrigant

Group Type EXPERIMENTAL

endoactivator

Intervention Type DEVICE

activation of irrigant during root canal treatment

One group will receive irrigation during root canal treatment in which activation will not occur

This group consists of patients who will receive irrigation during root canal treatment using the conventional syringe irrigation technique without the use of the EndoActivator system.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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endoactivator

activation of irrigant during root canal treatment

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* irreversible pulpitis
* symptomatic apical periodontitis
* asymptomatic apical periodontitis
* compliant patients
* sufficient ferrule for post operative restoration

Exclusion Criteria

* periapical abcess
* severe periodontal disease with guarded periodontal prognosis
* teeth with guarded post operative restoration prognosis
* non compliant patients
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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CMH Lahore Medical College and Institute of Dentistry

OTHER

Sponsor Role lead

Responsible Party

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Samia Rasool

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Imran Khan, BDS FCPS

Role: STUDY_DIRECTOR

28 military dental centre

Locations

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28 Military Dental Centre

Lahore, Punjab Province, Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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107/Civ/Trg/Op/15/24

Identifier Type: -

Identifier Source: org_study_id

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