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A STUDY TO SEE THE EFFECTS OF PLACING A MATERIAL MADE OF PATIENTS OWN BLOOD IN IMPLANT PLACED IMMEDIATELY AFTER REMOVAL OF TOOTH

Phase 3
Not yet recruiting
Conditions
non- restorable tooth or root stumps
Retained 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
Inclusion Criteria
  • 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.
Exclusion Criteria
  • 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
NameTimeMethod
1.Tissue biotype assessmentAFTER 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
NameTimeMethod
1.Modified Plaque index2. 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, India
Dr Monal Soni
Principal investigator
8219503382
monalsoni.ms@gmail.com

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