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3D Printed PEEK Implants for Cranioplasty

3D Printed PEEK Implants for Cranioplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05291754
Acronym
PEEKCP
Enrollment
40
Registered
2022-03-23
Start date
2021-11-26
Completion date
2026-03-26
Last updated
2026-01-21

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

Conditions

Skull Defect

Keywords

PEEK, Cranioplasty, 3D printer

Brief summary

This study is a non-randomised and single center study with patients needing an artificial skull bone eg cranioplasty. 40 patients will be implanted with in house manufactured polyether ether ketone (PEEK) implants using a fused filament fabrication 3D printer. The primary aim is to ascertain safety and feasibility of the procedure. The secondary aim is to compare complication rates with conventional methods such as autologous bone and polymethylmetacrylate (PMMA).

Detailed description

Cranioplasty is the surgical repair of a congenital or cranial defects after head trauma, infection or decompressive craniectomy. Although some patients can tolerate cranial defects for varied periods of time, cranioplasty is mostly indicated due to the increased risk of additional brain trauma, local pain or impaired CSF circulation but also aesthetic and psychological issues. The gold standard for repair since many years is cranioplasty with autologous bones . However, sometimes it not feasible to use the patient's autologous bone due to infections, trauma, bone graft resorption and donor-site morbidity. To replace the autologous bone grafts several different materials have been used, or are in use, as titanium meshes, hydroxyapatite cement and plastic resins as polymethyl methacrylate (PMMA) and porous polyethylene. Some of these have gathered increased interest due to advancements in technology for manufacture of these materials, and also the possibility to create custom made implants or moulds. The present study aims to assay safety and feasibility of in house 3D printed medical grade PEEK implants in research persons with acquired skull defects. The implants will be manufactured after 3D rendering from CT images of the skull defects, sterilised and aseptically inserted in the defects by means of a surgical intervention. A safety interim analysis will be performed after inclusion of 10 patients.

Interventions

3D printed PEEK skull implant

Sponsors

Skane University Hospital
Lead SponsorOTHER
Region Skane
CollaboratorOTHER
Lund University
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Prospective, non randomised and single arm

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Scheduled for cranioplasty * Informed consent

Exclusion criteria

* No informed consent * Implant size greater than 12x12 cm

Design outcomes

Primary

MeasureTime frameDescription
Performed PEEK implantsAt end of surgical procedure, up to 2 months after inclusionPercentage of performed PEEK implants out of included patients.
Safety of PEEK implants1 yearSurvival percentage of PEEK implants. Will be compared to historical PMMA and autologous bone implants.

Secondary

MeasureTime frameDescription
Exposure time of PEEK implants compared to PMMA implants.During surgical procedure, up to 2 months after inclusion.Compare exposure time for PEEK implant during surgery with historical PMMA implants made in 3D printed mold.
Complications of PEEK implants12 monthsComplications after PEEK implants other than those leading to extraction of implant will be compared to historical PMMA and autologous bone implants.

Countries

Sweden

Contacts

STUDY_DIRECTOREinar Heiberg, MD, PhD

Skane University Hospital

Outcome results

None listed

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