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NCT04330768 Clinical Trial

Platelet Rich Fibrin(PRF) Injection for Treatment of Dental Pulp Exposure:Randomized Clinical Trial

Dental Caries Clinical Trial

Official title:
Platelet Rich Fibrin(PRF) Versus Pulp Capping in Treatment of Dental Pulp Exposure:Randomized Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04330768
Other study ID # 0555
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 2021
Est. completion date June 2022

Study information
Verified date March 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

platelet rich fibrin(PRF) obtained from patient from patient blood sample (before start of treatment)is injected in the site of exposure of exposure(intervention group) control group will receive normal pulp capping procedure by MTA follow up will be one year

Description:

intervention group:patient with deep caries lesion ,free from sign and symptoms of irreversible pulpitis the blood sample will be taken before the beginning of dental treatment..PRF will be obtained by blood centrifugal and injected in the site of exposure covered by glass ionomer restoration control group: patient with same condition will receive pulp capping procedure by MTA followed by glass ionomer restoration

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50
Est. completion date June 2022
Est. primary completion date March 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 45 Years
Eligibility Inclusion Criteria:

- deep carious lesion- no sign of irreversible pulpitis

Exclusion Criteria:

- old age- periapical lesion-

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• PRF pulp capping
PRF is injected in the site of exposure
• MTA pulp capping
conventional pulp capping procedure

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Outcome
Type Measure Description Time frame Safety issue
Primary pulp vitality no sign of irreversible pulpitis or pulpal necrosis After 1 year
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