Comparison Between PEEK With Platelet-rich Fibrin and PEEK Alone in Maxillary Sinus Augmentation

Comparison Between PEEK With Platelet-rich Fibrin and PEEK Alone in Maxillary Sinus Augmentation: Histomorphometric and Clinical Analysis: A Randomized Clinical Trial

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06376708

Enrollment

Registered

2024-04-19

Start date

2022-09-01

Completion date

2023-07-01

Last updated

2024-04-19

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

Conditions

Maxillary Sinus

Keywords

maxillary sinus elevation and PEEK

Brief summary

comparison between the resulted bone during maxillary sinus elevation by PEEK with and without platelet rich fibrin

Detailed description

Histomorphometric and clinical analysis of the bone formed after 6 months after the maxillary sinus elevation using PEEK in the 2 groups : the study group (PEEK with platelet rich fibrin) and the control group (PEEK alone ) .

Interventions

OTHERplatelet rich fibrin

platelet rich fibrin

OTHERPolyether ether ketone

Polyether ether ketone

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

SINGLE (Subject)

Intervention model description

use of platelet rich fibrin after maxillary sinus elevation using PEEK

Eligibility

Sex/Gender

ALL

Age

20 Years to 50 Years

Healthy volunteers

Inclusion criteria

* • Posterior edentulous ridges with pneumatized maxillary sinus and remaining bone height less than 4 mm. * ASA physical status I and II. * Patients willing to be a part of the study and ready to give their consent in writing for the same. * Patient not complain from maxillary sinusitis * Patient with good oral hygiene. * Both males as well as females without any active periodontal disease. * The edentulous ridges are covered with optimal thickness of mucoperiosteum with no signs of inflammation, ulceration or scar tissue. * Remaining natural teeth have good periodontal tissue support and occlusion showed sufficient inter arch space for future prosthesis.

Exclusion criteria

* • General contraindications to implant surgery. * Untreated gingivitis, periodontitis. * Subjected to irradiation in the head and neck area less than 1 year before implantation. * Untreated periodontitis. * Pregnant or nursing. * Unable to open mouth sufficiently to accommodate the surgical tooling. * Patients participating in other studies, if the present protocol could not be properly followed. * Patient who could/would not participate in the follow-up period.

Design outcomes

Primary

Measure	Time frame	Description
Bone quantity	6 months postoperatively	using of CBCT

Secondary

Measure	Time frame	Description
Bone quality	6 months postoperatively	Histomorphometic analysis (For Core biopsy)

Countries

Egypt

Outcome results

None listed

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