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

The Effects of Sonic Activation of Irrigant on Post Operative Pain After Root Canal Treatment on Permanent Dentition: A Randomized Clinical Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07062419
Enrollment
58
Registered
2025-07-14
Start date
2025-01-01
Completion date
2025-08-30
Last updated
2025-10-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Operative Pain, Root Canal Therapy

Brief summary

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

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.

Interventions

activation of irrigant during root canal treatment

Sponsors

CMH Lahore Medical College and Institute of Dentistry
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
post operative pain using endoactivatorbefore procedure, after 24 hours, 36 hours , 48 hours, 1 weekpost operative pain will be marked on visual analogue scale (VAS). the lower the score the less pain will be and vice versa. maximum score 10 minimum score 0 0 to 10 depicting no pain to worst pain
post operative painbefore procedure, after 24 hours , 36 hours , 48 hours , 1 weekpain will be evaluatedon visual analogue scale (VAS). the lower the score the less pain will be and vice versa. maximum score 10 minimum score 0 0 to 10 depicting no pain to worst pain

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026