Comparison of two plasma derivates as pulpotomy agents in human immature molars
- Registration Number
- CTRI/2020/06/025938
- Lead Sponsor
- Terna Dental College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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.
1. Uncontrolled bleeding during the amputation of coronal pulp tissue
2. Children with medical conditions or any associated systemic condition
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of clinical success of PRP and PRFTimepoint: 3 months
- Secondary Outcome Measures
Name Time Method Comparison of clinical and radiographic success of PRP and PRFTimepoint: 6 months and 12 months