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Enrolling By InvitationNCT06522321

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

Status
Enrolling By Invitation
Phase
Phase 2
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Krishnadevaraya College of Dental Sciences & Hospital · Academic / Other
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

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

Conditions

Interventions

TypeNameDescription
BIOLOGICALi-PRF and FDBAA mucoperiosteal flap will be raised and atraumatic extraction will be done. An immediate implant with FDBA and I-PRF (experimental group) will be placed according to the standard protocol. An immediate implant with FDBA( comparative group) will be placed according to the standard protocol . The surgical wound closure will be coapted with sutures

Timeline

Start date
2023-07-15
Primary completion
2024-08-25
Completion
2024-10-25
First posted
2024-07-26
Last updated
2024-07-30

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT06522321. Inclusion in this directory is not an endorsement.