Evaluation of the Effect of Different Irrigation Activation Methods During Endodontic Retreatment

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age13-60
SponsorMinia University

About this trial

The persistent and secondary intraradicular infections are the primary causes of post-treatment disease following endodontic treatment of any tooth. When conventional root canal treatment fails, endodontic retreatment is often the preferred option, as it represents one of the most conservative approaches.

Endodontic retreatment involves removing old root canal filling material followed by cleaning, shaping, and refilling the canals. It may be associated with postoperative pain due to periapical tissue irritation and apical extrusion of debris during instrumentation.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients with mature teeth.

Patients with failed previous Endo treatment related by periapical periodontitis

Single Rooted with single root canal.

Patients should be free from any systemic disease that may affect predictable outcome.

Disqualifiers

Patients with immature roots.

Patients with any systemic disease that may affect normal healing.

Patients with swelling.

Pregnant females.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Xp Finisher R file

    Procedure/Surgery

    to evaluate the incidence and severity of postoperative pain using a numeric rating scale at 24, 48, and 72 hours and periapical healing via CBCT following retreatment with two different irrigation activation techniques: 1. Xp Finisher R file activation of irrigation. 2. Ultrasonic activation of irrigation.

Treatment groups

34 Participants
are divided into 2 treatment groups
Group A: Xp Finisher R file GroupActive comparator 1 intervention
Group B: Ultrasonic activation GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Post Operative Pain

Assessing the post operative pain measured by a numerical pain rating scale (NRS) where the level of pain will be recorded as follows: 0 reading represents "no pain" ; 1- 3 reading represents "mild pain" ; 4- 6 reading represents "moderate pain" and 7- 10 reading representative sever pain.

Time frame
from 6 hours to 48 hours after the procedure

Secondary outcomes

Other outcomes

Sponsors and contacts

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