Efficacy of injectable platelet rich fibrin in immediate implant placement sites: A randomized controlled trial
Overview
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Subhashini Balaguru
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- thickness of gingiva
Overview
Brief Summary
purpose of the study is to access the efficacy of injectable platelet rich fibrin in immediate implant placement sites
Brief procedure
Atraumatic tooth extraction will be performed under local anesthesia
Extracted Socket will be assessed for Implant placement
The subjects who fulfill the inclusion criteria will be randomly assigned into following 2 groups using computer generated randomization
GROUP 1 (control group) 10 sites were treated with immediate implant placement with bone graft
GROUP 2(test group) 10 sites were treated with immediate implant placement with injectable platelet rich fibrin mixed with bone graft
The preparation of injectable platelet rich fibrin for the test group will be done by drawing 8 ml intravenous blood from the patient and collected into disposable plastic test tubes
As per Choukroun standard protocol centrifugation at 700rpm for 3min will be done
injectable platelet rich fibrin was created at upper level
It will be used along with DBM for test group
Both the groups will be assessed for clinical parameters
gingival biotype
peri implant probing depth and
radiographic parameters
marginal bone loss
peri implant radiolucency at baseline 1 4and 6months follow up
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- Outcome Assessor Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Age 18 to 65 years Good oral hygiene No acute infection Root fractures Grossly decayed roots Root resorptions Elians socket classification type I and II ASA PS I and II.
Exclusion Criteria
- •Smokers and alcoholics Pregnant and lactating women Presence of active infection Any periapical pathology Elians socket type III ASA PS III and above.
Outcomes
Primary Outcomes
thickness of gingiva
Time Frame: 6 months
peri-implant probing depth
Time Frame: 6 months
peri-implant radiolucency
Time Frame: 6 months
marginal bone level
Time Frame: 6 months
Secondary Outcomes
No secondary outcomes reported
Investigators
Subhashini Balaguru
SRM kattankulathur dental college