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A-prf,Nanochitosan Combined With A-prf Compared to Chitosan for Symptomatic Irreversible Pulpitis of Mature Teeth

Not Applicable
Recruiting
Conditions
Pulpitis - Irreversible
Interventions
Procedure: PULPOTOMY OF MATURE PERMENANT TEETH
Registration Number
NCT06438523
Lead Sponsor
Future University in Egypt
Brief Summary

Clinical and radiographic assessment of A-prf,A-prf combined with nanochitosan compared to chitosan for symptomatic irreversible pulpits in lower permanent first molar

Detailed Description

3 groups are allocated using : Aprf Aprf combined with nanochitosan Chitosan

Each group will be subjected to tests:

Tooth sensibility via EPT (electrical pulp tester)and thermal test Radiolucency in digital radiograph Pain in NRS(6-12-24-72h)for 1 week

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Patients suffering from Symptomatic irreversible pulpitis in mature mandibular molars only will be involved.

    • Patients of either gender aged from 15-30.
    • 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.
    • 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
  • Patients with immature roots.

    • 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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
chitosanPULPOTOMY OF MATURE PERMENANT TEETHhe access cavity will be prepared up to the level of pulp chamber floor using sterile round diamond bur size 1 in high-speed hand piece with coolant.Once the pulp has been reached, a sharp sterile excavator should be used to remove the pulp tissue to the level of the radicular/root canal orifices then chitosan will be applied
Advanced Platelet rich fibrin,A-prf,A-PRF scaffoldPULPOTOMY OF MATURE PERMENANT TEETHA-PRF will be prepared according to Choukroun's technique by drawing whole blood from the median cubital vein into a 10 ml plain plastic test tubes (non-citrated) without the addition of an anticoagulant reagent . To prevent the blood from coagulating, it will be centrifuged immediately using a table top centrifuge at 1500 rpm for 14 minute.
A-prf mixed with nano chitosanPULPOTOMY OF MATURE PERMENANT TEETHA-PRF will be prepared according to Choukroun's technique by drawing whole blood from the median cubital vein into a 10 ml plain plastic test tubes (non-citrated) without the addition of an anticoagulant reagent . To prevent the blood from coagulating, it will be centrifuged immediately using a table top centrifuge at 1500 rpm for 14 minute then mixed with nanochitosan
Primary Outcome Measures
NameTimeMethod
pain assessment6,12,24,72hours and 7 days postoperative

Pain assessment using numerical rate scale

Secondary Outcome Measures
NameTimeMethod
Clinical and radiographic success1,3,6,9and 12 months

It includes clinical and radiographic success if either of them failed the case will considered failed.

Clinical failure :signs and symptoms of inflammation or infection Radiograph success and failure based on periapical index

Trial Locations

Locations (1)

Future university

🇪🇬

Cairo, Fifth Settlement, Egypt

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