Clinical and Radiographic Assessment of Nano-Bioactive Glass Combined With I-PRF Scaffold in Vital Pulp Treatments in Mandibular Molars With Closed Apices
NCT ID: NCT05876520
Last Updated: 2023-05-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
28 participants
INTERVENTIONAL
2023-01-25
2024-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Total pulpotomy with I-PRF only
Total pulpotomy is done in mature permanent molars followed by I-prf application. Topped with BC putty for coronal seal, RMGI and restored with composite as final restoration
Total pulpotomy with I-prf mixed with Nano-bioactive glass
Total pulpotomy is done in mature permanent molars followed by I-prf mixed with Nano-Bioactive glass application. Topped with BC putty for coronal seal, RMGI and restored with composite as final restoration
Interventions
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Total pulpotomy with I-prf mixed with Nano-bioactive glass
Total pulpotomy is done in mature permanent molars followed by I-prf mixed with Nano-Bioactive glass application. Topped with BC putty for coronal seal, RMGI and restored with composite as final restoration
Eligibility Criteria
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Inclusion Criteria
* Tooth should give positive response to cold test
* Haemostasias should be achieved after total pulpotomy
* The tooth is restorable and free from advanced periodontal disease, cracks and splits.
* Patients should be free from any systemic disease that may affect normal healing and predictable outcome.
* Patients who will agree to the consent and will commit to follow-up period.
* Patients with mature root apices
* Patients with no internal or external resorption and no periapical lesions
* Soft tissues around the tooth are normal with no swelling or sinus tract.
Exclusion Criteria
* Haemostasias after 10 minutes can not be controlled after total pulpotomy
* Patients with any systemic disease that may affect normal healing.
* Patients with periapical lesions or infections.
* Pregnant females.
* Patients who could/would not participate in a 6 months follow-up.
* Patients with fistula or swelling
* Patients with necrotic pulp.
* Patients with old age.
14 Years
32 Years
ALL
Yes
Sponsors
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Cairo University
OTHER
Responsible Party
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Noor Mohammed Kamal Eldeen Ahmed Mohmammed Sayed
Resident of Endodontics
Principal Investigators
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Geraldine Ahmed
Role: STUDY_DIRECTOR
Vice Dean of Faculty of Dentistry Cairo University
Ahmed S. Elsheshtawy
Role: STUDY_CHAIR
Lecturer of Endodontics
Ayah Abdolwahab
Role: STUDY_CHAIR
Lecturer of Biomaterials
Noor K. Sayed
Role: PRINCIPAL_INVESTIGATOR
Resident of Endodontics
Locations
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Noor Mohammed Kamal Eldeen
Cairo, , Egypt
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ENDO-3-7-2
Identifier Type: -
Identifier Source: org_study_id
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