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Not yet recruiting NCT06913673

Postoperative Pain and Incidence of Extrusion Following the Use of Two Intra-canal Medications in Retreatment of Single Rooted Teeth

Phase II Interventional Endodontic Disease

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: Bio-c Temp, Metapex.
Who it may be relevant to
Registry conditions: Endodontic Disease. Basic parameters: 16 years — 40 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 →

Overview

This study aims to compare the postoperative pain and incidence of extrusion of two intracanal medications in the retreatment of single-rooted teeth. The main question it aims to answer is: Does the injection of intra-canal medication into the shaped root canal after complete removal of the old obturating material lead to post-operative pain and paste extrusion to periapical tissues or not?

Interventions

  • Other Bio-c Temp
    Intra-canal medication
  • Other Metapex
    Intra-canal medication

Primary outcome measures

  • Clinical assessment of the post retreatment pain. [Time frame: One week after re-treatment procdure]
  • Radiographic assessment of the extrusion of the paste into periapical tissues using Digital radiograph [Time frame: Immediate after retreatment]

Eligibility criteria

Inclusion criteria

  • Patients with failed endodontic treatment in single root teeth
  • Systemic free

Exclusion criteria

  • Muktirooted teeth

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: NCT06913673 · 1026/114

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗