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NCT Number: NCT05291754

3D Printed PEEK Implants for Cranioplasty

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).

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This study is active but is not currently recruiting participants.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Neurosurgery

Lund, 22185, Sweden

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Scheduled for cranioplasty
  • Informed consent

Exclusion criteria

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

Treatment and study plan

PEEK Cranioplasty

Device

3D printed PEEK skull implant

Primary outcomes

  1. Performed PEEK implants

    Time frame: At end of surgical procedure, up to 2 months after inclusion

    Percentage of performed PEEK implants out of included patients.

  2. Safety of PEEK implants

    Time frame: 1 year

    Survival percentage of PEEK implants. Will be compared to historical PMMA and autologous bone implants.

Secondary outcomes

  1. Exposure time of PEEK implants compared to PMMA implants.

    Time frame: 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.

  2. Complications of PEEK implants

    Time frame: 12 months

    Complications after PEEK implants other than those leading to extraction of implant will be compared to historical PMMA and autologous bone implants.

Sponsors and collaborators

Lead sponsor

Skane University Hospital

Other

Collaborators

  • Lund University
  • Region Skane

Registry information

Acronym: PEEKCP

Important dates

Study start
2021
Primary completion
2025
Study completion
2026
First posted
Mar 23, 2022
Registry last updated
Jan 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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