ClinicalTrials.Veeva

Menu

Postoperative Pain Evaluation After Obturation With Different Sealers

U

University of Siena

Status

Enrolling

Conditions

Pulpitis
Periapical Periodontitis
Necorsis

Treatments

Procedure: Continuous Wave Condensation
Procedure: AH Plus (Dentsply Sirona, Charlotte, NC, USA)
Procedure: NeoSealer Flo
Procedure: Single Cone Technique

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aims to evaluate the incidence and intensity of postoperative pain in patients undergoing root canal treatment on teeth diagnosed with pulpitis, pulp necrosis, or with previous endodontic treatment. Teeth will be obturated using either bioceramic or resin-based sealers. The primary objective is to determine whether the type of sealer significantly influences the level of postoperative pain as reported by patients. Pain intensity will be assessed using the Visual Analogue Scale (VAS) at three time points: immediately after treatment, 24 hours, and 72 hours postoperatively. The findings are expected to provide clinical insight into which obturation material may be more effective in minimizing postoperative discomfort.

Enrollment

270 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients aged 18 years and older. Teeth with a diagnosis of pulpal necrosis or irreversible pulpitis. Informed consent provided for data usage.

Exclusion criteria

  • Patients with systemic conditions that may impair healing (e.g., uncontrolled diabetes, immunosuppression).
  • Asymptomatic presentation
  • Teeth with root fractures, resorption, or open apices.
  • Incomplete clinical or radiographic records.
  • Cases with poor-quality radiographs or lack of standardization for evaluation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

270 participants in 4 patient groups

Active Comparator: AH Plus + Continuous Wave Condensation
Active Comparator group
Description:
Root canal obturation using AH Plus (Dentsply Sirona, Charlotte, NC, USA) and the continuous wave technique with thermoplasticized gutta-percha
Treatment:
Procedure: AH Plus (Dentsply Sirona, Charlotte, NC, USA)
Procedure: Continuous Wave Condensation
Active Comparator: AH Plus + Single Cone
Experimental group
Description:
Root canal obturation using AH Plus and the single cone technique with cold gutta-percha.
Treatment:
Procedure: Single Cone Technique
Procedure: AH Plus (Dentsply Sirona, Charlotte, NC, USA)
NeoSealer Flo + Continuous Wave
Experimental group
Description:
Root canal obturation using NeoSealer Flo (Avalon Biomed, Houston, TX, USA) and the continuous wave technique.
Treatment:
Procedure: NeoSealer Flo
Procedure: Continuous Wave Condensation
NeoSealer Flo + Single Cone
Experimental group
Description:
Root canal obturation using NeoSealer Flo and the single cone technique.
Treatment:
Procedure: Single Cone Technique
Procedure: NeoSealer Flo

Trial contacts and locations

1

Loading...

Central trial contact

Giulia Malvicini, DDS

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems