Clinical Trial Details
— Status: Active, not recruiting
Administrative data
| NCT number |
NCT05427643 |
| Other study ID # |
964_07706223546 |
| Secondary ID |
|
| Status |
Active, not recruiting |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
December 15, 2021 |
| Est. completion date |
May 2023 |
Study information
| Verified date |
June 2022 |
| Source |
University of Baghdad |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
the main aim of the study is to evaluate the secondary implant stability when using dental
implants with injectable platelet rich fibrin accompanied by non-autogenous bone graft
material in narrow ridge cases versus straightforward ridges , in clinical comparative study.
Description:
the main aim of the study is to evaluate the secondary implant stability when using dental
implants with injectable platelet rich fibrin accompanied by non-autogenous bone graft
material in narrow ridge cases versus straightforward ridges , in clinical comparative study.
Study design:
Forty implants will be installed for this prospective clinical study, the implants will be
equally divided into two groups.
Group A (control group) in which the implants will be installed in a straightforward cases.
Group B (study group) in which the implants will be installed by utilizing injectable PRF
with non-autogenous bone graft material in narrow ridges.
Preparation of Injectable Platelet Rich Fibrin for the narrow ridge cases is as following:
Five ML of autologous blood to be collected from the forearm (median cubital vein \ cephalic
vein \ basilic vein ) by needle gauge with a 5mL sterile syringe without anticoagulant. The
entire blood is moved to a 5 milliliter plastic tube, directly centrifugated for 3 minutes at
700 rpm/min at room temperature. A liquid form ( Injectable PRF ) is then achieved on top of
the tube just and the red corpuscles at the bottom. Subsequently, the Injectable PRF liquid
form is collected from the tube by a sterile plastic syringe, Then it will be mixed with
non-autogenous bone graft waiting for 4min, and applied in the area with narrow ridge(
deficiency in the horizontal bone width ) .
Follow up Twenty four weeks after surgery , The uncoverage surgery is done under L.A using a
tissue paunch for installing the healing abutment ( gingival former ) , Then the secondary
stability of implant (Osseointegration) is to be measured using the (Anycheck ) device , and
comparing the 2 groups
