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Enrolling by invitation NCT06976411

Evaluation for Healing of Iatrogenic Perforation After Repair With Different Materials

Phase IV Interventional Root Perforation at the Bifurcation Area

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: MTA, Bioceramic putty.
Who it may be relevant to
Registry conditions: Root Perforation at the Bifurcation Area. Basic parameters: 15 years — 50 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
Egypt
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

Prospective Evaluation for Healing of Iatrogenic Perforation After Repair With Different Materials

Overview

The goal of this clinical trial is to evaluate healing potentiality of MTA and bioceramics materials as a root perforation repair material. The main questions it aims to answer are: is there is a significant difference in healing potentiality of MTA and bioceramics materials as a root perforation repair material? Participants will: enrollment will be from out-patients clinic of endodontic department, faculty of dentistry, Ain Shams university with root perforations. perforation repair will be done using either bio-ceramic or MTA repair material and preoperative or immediate postoperative CBCT and postoperative CBCT will be taken to compare healing.

Interventions

  • Drug MTA
    Perforation repair using MTA repair material
  • Drug Bioceramic putty
    Perforation repair using Bioceramic repair material

Primary outcome measures

  • Radiographic success in terms of healing [Time frame: 1 year]
  • patients with clinical success [Time frame: 1 year]

Eligibility criteria

Inclusion criteria

  • Patients with root perforation in lower molars.
  • Patients had anon contributory medical history.
  • Patients of age categories between 15 to 50 years old.
  • No sex restriction.
  • Small to medium size perforation.

Exclusion criteria

  • Patients with generalized chronic periodontitis.
  • Teeth with difficult isolation.
  • Non restorable teeth.
  • Medically compromised patients.
  • Patients with history of allergies to any of the medications to be used during or after the treatment.

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

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Faculty of dentistry ain shams university — Cairo

Identifiers

NCT: NCT06976411 · FDASU-REC 1117 pro

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗