A STUDY TO SEE THE EFFECTS OF PLACING A MATERIAL MADE OF PATIENTS OWN BLOOD IN IMPLANT PLACED IMMEDIATELY AFTER REMOVAL OF TOOTH
- Conditions
- non- restorable tooth or root stumpsRetained dental root,
- Registration Number
- CTRI/2021/04/032917
- Lead Sponsor
- MONAL SONI
- Brief Summary
OBJECTIVE- To evaluate the hard and soft tissue outcome of immediate implant placement with or without L-PRF.
METHODOLOGY- A total of 18 immediate implants were placed. Patients were divided into two groups i.e. immediate implants with L-PRF (n=9) and immediate implants without L-PRF (n=9). The patients received a definitive restoration after 3 months of immediate implant placement and were followed up for a period of 6-months.
RESULT- There was significant improvement seen in tissue biotype, probing depth & marginal bone loss in test group as compared to control group.
CONCLUSION- Immediate placement of implants with L-PRF membrane could be considered a valuable option to replace missing tooth with hard and soft tissue regeneration. But, this study looked at very few cases over a limited period. Thus, long-term clinical studies are needed to validate the findings.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 18
- 1.Patient with age group between 18-65 years.
- 2.Patient, who are cooperative, motivated and with good oral hygiene.
- 3.Patients with no acute infection.
- 4.Patients with sufficient bone volume at the site of immediate implant placement.
- 5.Patients who are willing and available for recall follow ups.
- 7.Teeth indicated for extraction due to causes like root fracture, grossly decayed, root resorption etc.
- 1.Patient unable to maintain adequate oral hygiene.
- 2.Patients with any known systemic disease/conditions and/or on medication known to interfere with wound healing.
- 3.Patients who are current smokers or consume any other form of tobacco.
- 4.Patients with para-functional habits & traumatic occlusion.
- 5.Patients with severe malocclusion or crowding.
- 6.Teeth with periapical pathologies.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Tissue biotype assessment AFTER 10 DAYS, 1 MONTH, 3 MONTHS AND 6 MONTHS 2. Radiographic evaluation (standardized Periapical radiograph with grid) for peri-implant bone loss and radiolucency. AFTER 10 DAYS, 1 MONTH, 3 MONTHS AND 6 MONTHS Primary outcome: evaluation will be done clinically and radiographically. AFTER 10 DAYS, 1 MONTH, 3 MONTHS AND 6 MONTHS
- Secondary Outcome Measures
Name Time Method 1.Modified Plaque index 2. Modified sulcus bleeding index
Trial Locations
- Locations (1)
J.N. Kapoor D.A.V Dental College
🇮🇳Yamunanagar, HARYANA, India
J.N. Kapoor D.A.V Dental College🇮🇳Yamunanagar, HARYANA, IndiaDr Monal SoniPrincipal investigator8219503382monalsoni.ms@gmail.com