Postoperative Pain and Success of Single-Visit Root Canal Treatment Using Different Root Canal Sealers in Asymptomatic Teeth

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorIstanbul Medipol University Hospital

About this trial

This study evaluates the postoperative pain and long-term clinical and radiographic success of single-visit primary root canal treatment in asymptomatic teeth with periapical lesions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged 18-65 years.

Teeth that have not previously undergone root canal retreatment or surgical intervention.

Patients who are able to read and sign the informed consent form.

Patients who are physically and mentally able to tolerate the planned dental treatment.

Disqualifiers

Pregnant or lactating women.

Patients with chronic periodontal disease and/or a periodontal probing depth >4 mm.

Symptomatic patients.

Patients who are unable to comply with the scheduled follow-up periods.

Trial design

Design model

Parallel

Treatments tested in this trial

  • One-Fill

    Other intervention

    Root canal obturation using One-Fill bioceramic sealer with a single-cone technique. The prepared root canal is filled with a fitted gutta-percha cone coated with One-Fill sealer according to the manufacturer's instructions.

  • TotalFill

    Other intervention

    Root canal obturation using TotalFill BC Sealer with a single-cone technique. The prepared root canal is filled with a fitted gutta-percha cone coated with TotalFill BC Sealer according to the manufacturer's instructions.

  • AH Plus + Single Cone

    Other intervention

    Root canal obturation using AH Plus epoxy resin-based sealer with a single-cone technique. A fitted gutta-percha cone is coated with AH Plus sealer and placed to the working length according to the study protocol.

  • AH Plus + Continuous Wave

    Other intervention

    Root canal obturation using AH Plus epoxy resin-based sealer with the continuous wave of condensation technique. The master gutta-percha cone is fitted to the working length, followed by down-pack and backfill procedures using heated gutta-percha according to the study protocol.

Treatment groups

200 Participants
are divided into 4 treatment groups
Group A: One FillExperimental treatment 1 intervention
Group B: TotalFillExperimental treatment 1 intervention
Group C: AH Plus + Single ConeExperimental treatment 1 intervention
Group D: AH Plus + Continuous WaveExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Postoperative Pain

Postoperative pain following single-session primary root canal treatment, assessed using a 10-point visual analog scale (VAS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. higher scores indicate greater pain intensity.

Time frame
6 hours, 24 hours, 48 hours, 72 hours, 1 week, 1 month after root canal treatment.
2

Clinical Success and Radiographic Radiographic Changes in Periapical Lesion Size Following Root Canal Treatment

Radiographic assessment of periapical lesion size following single-session primary root canal treatment. Periapical lesion size will be measured on digital periapical radiographs using image analysis software. A coin of known diameter will be used as a radiographic calibration reference to standardize measurements. The maximum diameter of the periapical radiolucency will be measured in millimeters (mm) at each follow-up examination (1, 3, 6, and 12 months). Changes in lesion size will be calculated by comparing measurements obtained at baseline and subsequent follow-up examinations.

Time frame
1 months / 3 months /6 months / 12 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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