None listed
Conditions
Interventions
Intervention1: Platelet Rich Plasma: One ml of peripheral venous blood will be drawn from the patientâ??s median cubital vein and transferred into a sterile evacuated 10 ml tube containing acetic acid
top-most platelet poor plasma (PPP) layer, middle buffy layer, and bottom- most red blood cell layer. Using a sterile micro pipette, the PPP and buffy layer will be collected in a 5ml sterile glass tu
platelet poor plasma at the surface, PRF clot in the middle, and red blood cells at the bottom. Sterile tweezers will be inserted into a test tube to retrieve the PRF clot. The platelet fibrin membran
Sponsors
Terna Dental College
Eligibility
Inclusion criteria
Inclusion criteria: 1. Large carious or mechanical exposure (more than 1 mm) of the vital coronal pulp 2. Absence of symptoms indicative of advanced pulpal inflammation such as spontaneous pain or history of nocturnal pain 3. Absence of clinical signs or symptoms suggesting a nonvital tooth such as suppurating sinus, soft tissue swelling. 4. Restorable tooth structure. 5. Bleeding should be controlled from the amputated pulp stumps within 5 minutes using sterile moist cotton pellets. 6. No evidence of external and/or internal root resorption 7. No widening of periodontal ligament (PDL) space 8. Absence of furcal or periapical radiolucency 9. Absence of canal calcification or pulp stone.
Exclusion criteria
Exclusion criteria: 1. Uncontrolled bleeding during the amputation of coronal pulp tissue 2. Children with medical conditions or any associated systemic condition
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of clinical success of PRP and PRFTimepoint: 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of clinical and radiographic success of PRP and PRFTimepoint: 6 months and 12 months | — |
Countries
India
Contacts
Public ContactDr Devendra Patil
Terna Dental College
Outcome results
None listed