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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

EVALUATION OF THE CLINICAL AND RADIOGRAPHIC EFFECTS OF L-PRF MEMBRANE IN IMMEDIATE POST EXTRACTION IMPLANT PLACEMENT A RANDOMIZED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032917
Enrollment
18
Registered
2021-04-19
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K083- Retained dental root

Interventions

Intervention1: L-PRF: PRF membrane will be transferred with PRF forceps to sterile PRF tray to use it at the immediate implant placement site. The membrane will be then taken to surgical site at time

Sponsors

MONAL SONI
Lead Sponsor

Eligibility

Inclusion criteria

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. 6.Teeth indicated for extraction with terminal periodontal disease. 7.Teeth indicated for extraction due to causes like root fracture, grossly decayed, root resorption etc.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Primary outcome: evaluation will be done clinically and radiographically. 1.Tissue biotype assessment 2. Radiographic evaluation (standardized Periapical radiograph with grid) for peri-implant bone loss and radiolucency. Timepoint: AFTER 10 DAYS, 1 MONTH, 3 MONTHS AND 6 MONTHS

Secondary

MeasureTime frame
1.Modified Plaque index 2. Modified sulcus bleeding index 3.Peri-implant pocket depth 4.Implant stability Timepoint: AFTER 10 DAYS, 1 MONTH, 3 MONTHS AND 6 MONTHS

Countries

India

Contacts

Public ContactDr MONAL SONI

DAV DENTAL COLLEGE

drshalinigugnani@gmail.com9466949150

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026