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Effect of Different NanoScaffolds on Pulp Regeneration in Non-Vital Immature Permanent Teeth (Randomized Clinical Trial)

Effect of Different NanoScaffolds on Pulp Regeneration in Non-Vital Immature Permanent Teeth (Randomized Clinical Trial)

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07121348
Acronym
Regeneration
Enrollment
40
Registered
2025-08-13
Start date
2025-07-28
Completion date
2026-12-01
Last updated
2025-08-13

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

Conditions

Necrotic Immature Permanent Incisors

Brief summary

the clinical trial aims to evaluate efficency of different scaffolds in cases of regeneration

Detailed description

The aim of this study is to evaluate the clinical and radiographic outcome of regenerative endodontic procedures in immature non-vital permanent teeth using different nanoscaffolds (Platelet-rich fibrin, Mesoporous silica nanoparticles, Hyaluronic acid nanoparticles, Pomegranate nanoparticles)

Interventions

PROCEDUREPlatelet rich fibrin

platelet rich fibrin is obtained by removing the middle layer from a centrifuged blood sample and is rich with platelets that plays an important role in tissue regeneration mesoporous silica nanoparticles are high surface area and excellent biocompatibility and enhance the outcome hyalurnic acid nanoparticles are high water capacity and involved in cell proliferation and adhesion and help in tissue regeneration pomegranate nanoparticles has anti-inflammatory and antibacterial effect and also help in tissue proliferation and regeneration

Sponsors

Tanta University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
9 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

• Patients free from any systemic diseases that may interfer with the normal healing process. * Maxillary traumatized or cariously exposed non-vital immature anterior teeth. * Teeth don't need for post and core as a final restoration. * Radiographic evidence of an apical opening width more than 2 mm with or without periapical radiolucency. * Teeth without anatomical variations

Exclusion criteria

• Immunocompromised patients * Teeth with previous endodontic treatment. * Teeth with internal or external resorption * Radiographic evidence of root fracture. * Lack of patient and parent cooperation. * Presence of periodontal pocket depth more than 4 mm.

Design outcomes

Primary

MeasureTime frameDescription
apical closure assessed radiographically12 months after treatmentradiographic evaluation of apical closure as reduction or elimination of the apical opening of the root

Countries

Egypt

Outcome results

None listed

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