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Patient Specific PEEK Versus Titanium Patient Specific Plates in The Fixation of Computer-Guided Advancement Genioplasty

Patient Specific Polyetheretherketone (PEEK) Miniplates Versus Titanium Genioplasty Plates in The Fixation of Computer-Guided Advancement Genioplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06838533
Acronym
PEEK
Enrollment
14
Registered
2025-02-20
Start date
2018-03-03
Completion date
2024-10-01
Last updated
2025-02-27

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

Conditions

Mandible; Deformity

Keywords

Genioplasty, PEEK, Mandible deformity

Brief summary

Evaluation of polyetheretherketone (PEEK) versus titanium patient specific plates in the fixation of computer-guided advancement genioplasty.

Detailed description

Aim: Comparison between polyetheretherketone (PEEK) and titanium patient specific plates in the fixation of computer-guided advancement genioplasty. Patients and Methods: This study included fourteen patients indicated for advancement genioplasty. Patients were assigned randomly into one of two equal groups. Group A (Control group) included seven patients who were treated by computer guided advancement genioplasty using patient specific titanium plates and Group B(Study group) involved seven patients who were treated by computer guided advancement genioplasty using patient specific PEEK plates.

Interventions

PEEK vs Titanium patient specific plates

Sponsors

Faculty of Dental Medicine for Girls
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
17 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Patients who are indicated to advancement genioplasty. * Patients with completed growth. * Physically and psychologically able to tolerate surgical procedures.

Exclusion criteria

* Presence of any medical conditions that contraindicate the surgical procedure. * Any medical condition that compromises the healing and surgical outcome.

Design outcomes

Primary

MeasureTime frameDescription
Stability of PEEK vs Titanium plates6 months follow upRadiographic linear discrepancy in mm (Horizontal and vertical) between Pogonion and Menton position in immediate and 6 months postoperative

Secondary

MeasureTime frameDescription
Cost of patient specific plated (PEEK and titanium)6 monthsNumber in Egyptian pound
Soft tissue healing6 monthsBinary answer (yes if happened or no if not happened) of clinical examination (Infection, soft tissue dehiscence and plate exposure)
Patient satisfaction6 monthsNumber from 1 to 5 of a 5-point Likert scale (1 very dissatisfied is minimal to 5 very satisfied is maximum)

Countries

Egypt

Outcome results

None listed

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