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Assessment of Postoperative Pain Following Root Canal Obturation of Permanent Mature Teeth Using Three Different Obturation Techniques: A Randomized Clinical Trial

ConditionPostoperative Pain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorTanta University

About this trial

purpose: to evaluate the postoperative pain incidence and intensity after three different obturation techniques (Cold lateral condensation technique (CLC), Vibration thermo-dynamic technique (Vibra-Tho) and Injection of thermo-plasticized gutta-percha (Fast Fill device)). Materials and Methods: Thirty patients with non-vital mature maxillary incisors requiring endodontic treatment will be randomly divided into three groups (n=10) according to the obturation technique used: Group I (CLC), Group II (Vibra-Tho) and Group III (Fast Fill device). Postoperative pain levels will be recorded using the visual Analogue Scale (VAS) immediately post operative and at 24 hours, 72 hours, one week and two weeks.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients with single rooted mature permanent teeth

presence of symptomatic or asymptomatic irreversible pulpitis or apical periodontitis

medically free patients

Disqualifiers

Teeth with previous root canal treatment teeth with anatomical variations patients who take analgesic or antiinflammatory drugs regularly or just before participation in the study

Trial design

Design model

Parallel

Treatments tested in this trial

  • Cold Lateral condensation technique

    Procedure/Surgery

    Root canal obturation technique

  • Vibration thermo-dynamic technique

    Procedure/Surgery

    a device for obturation of root canal

  • Injection of thermo-plasticized gutta-percha

    Procedure/Surgery

    a device for root canal obturation

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: Cold lateral condensation techniqueExperimental treatment 1 intervention
Group B: Vibration thermo-dynamic techniqueExperimental treatment 1 intervention
Group C: Injection of thermo-plasticized gutta-perchaExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Postoperative pain

postoperative pain will be evaluated using VAS

Time frame
post operative and at 24 hours, 72 hours, one week and two weeks.

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Tanta University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: