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

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Maxillary Sinus

Treatments

Other: platelet rich fibrin
Other: Polyether ether ketone

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Full 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 ) .

Enrollment

24 patients

Sex

All

Ages

20 to 50 years old

Volunteers

No 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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

24 participants in 2 patient groups

PEEK and PRF
Experimental group
Description:
maxillary sinus elevation using PEEK and platelet rich fibrin
Treatment:
Other: Polyether ether ketone
Other: platelet rich fibrin
PEEK alone
Active Comparator group
Description:
maxillary sinus elevation using PEEK alone
Treatment:
Other: Polyether ether ketone

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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