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

Ain Shams University

Status

Completed

Conditions

Bone Loss

Treatments

Other: injectable platelet rich fibrin

Study type

Interventional

Funder types

Other

Identifiers

NCT04298294

Bassant Mohye

Details and patient eligibility

About

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

Full 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.

Enrollment

16 patients

Sex

All

Ages

20 to 50 years old

Volunteers

Accepts Healthy Volunteers

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.