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Assessment of L-PRF, Nanohydroxyapatite Combined With L-PRF Using Pulpotomy in Mature Mandibular First Molars

Not Applicable
Recruiting
Conditions
Irreversible Pulpitis
Registration Number
NCT06613932
Lead Sponsor
Future University in Egypt
Brief Summary

Clinical and Radiographic Assessment of L-PRF, Nanohydroxyapatite material combined with L-PRF scaffold in Vital pulp Therapy. Treatments in Mandibular First Molars with Closed Apices, Randomized Controlled Trial.

Detailed Description

pulpotomy by using 3 materials. The first group(control group ) uses hydroxyapatite material as a pulpotomy agent, and the second group uses L-PRF as a pulpotomy agent. the third group uses combined material (L-PRF = Nano hydroxyapatite )as a pulpotomy agent .. then assesses the clinical and radiographic result of the 2 interventions group with control group

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
45
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
post operative Pain assessment6, 12, 24, 72hours and 7 days after treatment

Pain evaluations were conducted preoperatively with numerical rating scale ( a verbal or writing determination of a pain level on a scale from 0 to 10, in which 0 represents no pain and 10 represents excruciating pain .

Secondary Outcome Measures
NameTimeMethod
Dentine bridge formation12 months post operative

evaluating the thickness of dentine bridge formed after the procedure by comparing immediate post operative CBCT with the one year follow up scans

Trial Locations

Locations (1)

future university in Egypt

🇪🇬

Cairo, New Cairo, Egypt

future university in Egypt
🇪🇬Cairo, New Cairo, Egypt
nada A metwally, master
Contact
01122289353
nadaaymaan55@gmail.com

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