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

C

CMH Lahore Medical College and Institute of Dentistry

Status

Completed

Conditions

Root Canal Therapy
Post Operative Pain

Treatments

Device: endoactivator

Study type

Interventional

Funder types

Other

Identifiers

NCT07062419
107/Civ/Trg/Op/15/24

Details and patient eligibility

About

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.

Full description

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.

Enrollment

58 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

58 participants in 2 patient groups

one group will receive irrigation during root canal treatment will be activated by an Endoactivator
Experimental group
Description:
activation of an irrigant by using certain ultrasonic frequency to enhance antimicrobial action of irrigant
Treatment:
Device: endoactivator
One group will receive irrigation during root canal treatment in which activation will not occur
No Intervention group
Description:
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.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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