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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06762821
Enrollment
86
Registered
2025-01-08
Start date
2024-12-21
Completion date
2027-03-31
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Necrotic Immature Permanent Incisors

Keywords

single-visit

Brief summary

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

PROCEDURESingle-visit revascularization

Revascularization protocol will be performed in single visit

PROCEDUREMultiple-visit revascularization

Revascularization protocol will be performed in multiple visit

Sponsors

Minia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

biostatistician

Eligibility

Sex/Gender
ALL
Age
7 Years to 13 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants experiencing Pain after treatmentFrom enrollment to the end of treatment at 24 monthsZero is equivalent to no pain and 1 indicates presence of pain that necessitate taking pain killer

Countries

Egypt

Contacts

Primary ContactGad El-Hak, Lecturer
osama.seif@mu.edu.eg00201023449797

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026