Menu
Not yet recruiting NCT07574801

Postoperative Pain Following Root Canal Treatment With Bioceramic Sealers

No phase Interventional Root Canal Treatment Irreversible Acute Pulpitis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: root canal treatment, root canal treatment.
Who it may be relevant to
Registry conditions: Root Canal Treatment, Irreversible Acute Pulpitis. Basic parameters: 18 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Postoperative Pain and Sealer Extrusion Following Root Canal Treatment With Neosealer Flo and Ceraseal Bioceramic Sealers; a Randomized Clinical Trial

Overview

To evaluate and compare postoperative pain and extrusion of sealers following root canal treatment using NeoSealer Flo and CeraSeal bioceramic sealers

Interventions

  • Procedure root canal treatment
    nanosealer flo bioceramic root canal sealer
  • Procedure root canal treatment
    cerseral bioceramic root canal sealer

Primary outcome measures

  • postoperative pain [Time frame: 24 and 48 hours]
Secondary outcome measures (1)
  • sealer extrusion [Time frame: immediate postoperatively]

Eligibility criteria

Inclusion criteria

  • Molar teeth requiring root canal treatment
  • Diagnosed with symptomatic irreversible pulpitis,
  • Patients able to understand and use the VAS scale

Exclusion criteria

  • Patients with systemic diseases affecting pain perception
  • Use of analgesics within 12 hours before treatment
  • Previously treated teeth
  • Teeth with periapical abscess or swelling

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07574801 · NewENDO3.3.3

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗