Effect of Different Sealers and Activation Methods on Pain

ConditionChronic Apical Periodontitis

Trial statusNot yet recruiting

Trial phasePhase 4

Trial typeInterventional

Biological sexAll

Age18-60

SponsorTC Erciyes University

About this trial

In this study, the effects of different irrigation agitation methods and different root canal filling sealers on postoperative pain after root canal treatment will be evaluated.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients aged 18-60 years who are classified as medically healthy (ASA I or II),

Teeth that do not need periodontal and prosthetic treatment, with a periapical index score between 2 and 4,

Teeth with single root and canal diagnosed with asymptomatic apical periodontitis,

Teeth that respond negatively to electric pulp test (Parkell) or cold test (Endo Ice; Coltene, Altstätten, İsviçre), without pain during percussion and palpation.

Disqualifiers

Teeth with PAI scores lower than 2

Patients who had taken analgesics or anti-inflammatory drugs in the last 4 hours

Diabetic, immunocompromised, pregnant or history of antibiotic use in the last month or patients receiving antibiotic prophylaxis

Teeth with root resorption, immature, severe crown damage, calcified canals, and previous root canal fillings

Trial design

Design model

Parallel

Treatments tested in this trial

Root Canal Sealants
Drug
In this study, different irrigation agitation methods and different root canal sealers will be compared.

Treatment groups

80 Participants

are divided into 4 treatment groups

Group A: Ah plus+MDAExperimental treatment 1 intervention

Group B: Ah plus+PUAExperimental treatment 1 intervention

Group C: Neosealer Flo+MDAExperimental treatment 1 intervention

Group D: Neosealer Flo+PUAExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

Pain symptoms of the patients will be evaluated with prepared questionnaires, and periapical lesion healing will be evaluated with periapical radiographs. A visual analog scale will be used to measure the degree of pain.

Performing clinical and radiographic follow-up and evaluation of the patient.A visual analog scale will be used to measure the degree of pain.

Time frame

1-4 months

Locations

This trial has no locations.

Sponsors and contacts

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

TC Erciyes University

Lead sponsor

Source ClinicalTrials.gov

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