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Radiographic Assessment of Bone Dimension Around Immediate Implants With FDBA and I-PRF vs FDBA Alone | Clinical Trials | Clareo Health

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Radiographic Assessment of Bone Dimension Around Immediate Implants With FDBA and I-PRF vs FDBA Alone

Radiographic Assessment of Bone Dimension Around Immediate Implants With FDBA and I-PRF vs FDBA Alone- A Randomized Clinical Controlled Trial

NCT06522321•Krishnadevaraya College of Dental Sciences & Hospital

View on ClinicalTrials.gov

Summary

The present study is a human, prospective, parallel, randomised controlled clinical trial conducted for radiographic assessment of bone dimension around immediate implants with FDBA and I-PRF vs FDBA Alone The trial is in accordance with the Consolidated Standards of Reporting Trials (CONSORT) criteria, 2010.

Detailed Description

Twenty healthy individuals satisfying the inclusion and exclusion criteria were recruited for the study. A detailed, thorough medical and dental history was obtained and each patient was subjected to comprehensive clinical and radiological examination. All patients were informed about the nature of the study, the surgical procedure involved, potential benefits and risks associated with the surgical procedure and written informed consent were obtained from all patients. All the patients were treated with immediate implants in endodontically and periodontically compromised sites. FDBA graft along with I-PRF is combined to form a sticky bone, this stable element is placed around the implants where bone is compromised. The clinical and radiographic parameters were recorded at baseline, three months and six months postoperatively

Eligibility

Age

18 - 55 years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•1. Patients between 18-55 years of age.
•2. Presence of non-restorable single rooted teeth (maxillary or mandibular) due to trauma, caries, root resorption, root fracture, endodontic or periodontal failure.
•3. Grade I or Grade II extraction socket according to El Chaar et al 2016.
•4. Good oral hygiene.
•5. Good patient compliance.

Exclusion Criteria

•1. Systemic complications (uncontrolled diabetes and severe cardiovascular or infectious diseases).
•2. Intravenous and oral bisphosphonate therapy.
•3. Patients who are psychologically unable to participate.
•4. Pregnant patients, patients with bone diseases and patients on chemotherapy or radiotherapy, alcohol or drug abuse.
•5. Patients with hemorrhagic disorders.

Locations (1)

Dr. Prabhuji MLV

Bengaluru, Karnataka, India

Key Dates

Start Date

July 15, 2023

Primary Completion Date

August 25, 2024

Completion Date

October 25, 2024

Last Updated

July 30, 2024

Enrollment

ESTIMATED participants

Conditions

Bone Density Increased

Interventions

i-PRF and FDBA

BIOLOGICAL

Bone Density in Immediate Implant Placment and Loading(BDIIPL)

NCT03626779

Bone Density Increased

View study

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: July 30, 2024Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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