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Recruiting NCT06762821

A 24-month Outcomes of Single- Vs Multiple-visit Revascularization

No phase Interventional Necrotic Immature Permanent Incisors

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: Single-visit revascularization, Multiple-visit revascularization.
Who it may be relevant to
Registry conditions: Necrotic Immature Permanent Incisors. Basic parameters: 7 years — 13 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 →
Official title

Clinical and Radiographic Outcomes of Single- Versus Multiple-visit Revascularization of Asymptomatic Necrotic Immature Maxillary Permanent Incisors: a 24-month Randomized Clinical Trial

Overview

The current randomized clinical trial will be conducted to evaluate the 24-month clinical and radiographic outcomes after revascularization of asymptomatic necrotic immature permanent maxillary incisors using single- or multiple-visit protocol.

Interventions

  • Procedure Single-visit revascularization
    Revascularization protocol will be performed in single visit
  • Procedure Multiple-visit revascularization
    Revascularization protocol will be performed in multiple visit

Primary outcome measures

  • Number of Participants experiencing Pain after treatment [Time frame: From enrollment to the end of treatment at 24 months]

Eligibility criteria

Inclusion criteria

  • Compliant healthy patients who had at least one immature maxillary permanent incisor requiring nonsurgical root canal treatment.
  • Patients presenting with a diagnosis of pulp necrosis with chronic apical periodontitis confirmed by history, clinical, radiographic and operative examination.
  • Patient without previous endodontic treatment in affected tooth.

Exclusion criteria

  • Patients with systemic conditions (medical, developmental or behavioral) that make routine dental treatment difficult.
  • Patients taking medications that can interfere with healing or hemostasis.
  • Patients with allergy to local anesthetics
  • Children who will not comply to recall program.
  • Teeth with extensive loss of coronal tissue that require restoration with a post
  • Teeth with internal or external root resorption

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
Single blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Minia University Dental Hospita — Minya

Identifiers

NCT: NCT06762821 · 20241220284

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗