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Synthetic Cranioplasty PEEK Versus UHMWP

NCT05250024 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2023-09-05

No results posted yet for this study

Summary

The purpose of this study is to report the investigators experience with synthetic reconstruction of cranial defects using computer guided milled UHMWP, in terms of benefits and limitations both clinically and radiographically in comparison to PEEK implants.

Conditions

  • Cranium; Deformity

Interventions

DEVICE

UHMWP Cranioplasty

patient specific cranial implant

DEVICE

PEEK Cranioplasty

patient specific cranial implant

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Mamdouh A Sayed, Professor · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
2 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-30
Primary Completion
2023-07-21
Completion
2023-07-21
FDA Device
Yes

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05250024 on ClinicalTrials.gov