Skip to content

Using of Injectable Platelet Rich Fibrin on Filling the Gap of Immediate Dental Implant

The Effect of Using of Injectable Platelet Rich Fibrin on Filling the Gap of Immediate Dental Implant in the Esthetic Zone

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04298294
Enrollment
16
Registered
2020-03-06
Start date
2018-02-16
Completion date
2019-12-01
Last updated
2020-03-06

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

Conditions

Bone Loss

Brief summary

The effect of using of i-PRF (injectable platelet rich fibrin) on filling the gap of immediate dental implant in the esthetic zone

Detailed description

Grouping the samples: (sixteen patients was recruited from the outpatient clinic of Oral Medicine, Periodontology, Diagnosis and Radiology Department, Faculty of Dentistry, Ain Shams University). The sixteen patients assigned to group 1 or group 2 will be randomly allocated using flip of a coin into one of the 2 treatment modalities. Primary objective: Radiograhic evaluation of the effect of i-PRF on filling the buccal gap distance between the immediately placed dental implant and the surrounding bone. Secondary objective: Esthetic evaluation of the effect of i-PRF on the soft tissue around immediately placed dental implant.

Interventions

biologic activator

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

double blinded

Intervention model description

Group I (study group)8 patients undergo flapless single immediate implant placement surgery with filling the gap distance with i-PRF& bone graft Group II (control group) 8 patients undergo flapless single immediate implant placement surgery with filling the gap distance with bone graft

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy adult patient. * Age from 20-50 years old * Patients must be free of any systemic disease which could influence the surgical procedure. * Tooth involved in the esthetic zone. * Sufficient hard and soft tissue volume in vertical and buccolingual 6. Natural teeth adjacent to the involved tooth were required to be free from infection. * Controlled oral hygiene. * Indication for tooth extraction included; * Endodontic failures * Untreatable caries\> Non- restorable teeth * Vertical root fracture * Remaining roots * The decision to proceed with the implant placement was made after tooth extraction and probing of the extraction socket which revealed: * The presence of intact facial bone. * Compliance with all requirements in the study and signing the informed consent.

Exclusion criteria

* Patient had surgeries in the same site during the last 6 months prior to the surgery. * Severe vertical bone loss (socket type lll or type lV). * Presence of acute dento-alveolar infection or periodontal affected of involved tooth. * Pregnant and lactating females. * Smokers.

Design outcomes

Primary

MeasureTime frameDescription
Radiograhic evaluation of the effect of i-PRF on filling the buccal gap distance between the immediately placed dental implant and the surrounding bone.6 months follow updensity, vertical and horizontal assessment of labial plate
Radiographic analysis6 months follow upvertical assessment of labial plate

Secondary

MeasureTime frameDescription
Esthetic evaluation of the effect of i-PRF on the soft tissue around immediately placed dental implant6 months follow uppink esthetic score

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026