Novel Head Protection Prototype Device for Decompression Craniectomy

NCT ID: NCT04021095

Last Updated: 2021-04-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-07-04
• Study Completion Date: 2021-03-31

Brief Summary

A proof-of-concept (POC) proposal to study the feasibility of customized head protection prototype device (HPPD) using 3D printed externally-applied moulded skin prosthesis integrated to the craniectomy bony skull defect.

Detailed Description

A proof-of-concept (POC) proposal to study the feasibility of customized head protection prototype device (HPPD) using 3D printed externally-applied moulded skin prosthesis integrated to the craniectomy bony skull defect. The proposed material is a bio-compatible, light-weight rigid /semi rigid material which can be fitted to the skull defect and interfaced with the subject's bony rim using soft, deformable material (e.g. silicon) and attached using an elastic head band or other acceptable means. The prosthesis is removable for skin and prosthesis cleansing and ventilation.

Study Specific Objectives:

(i) Primary Objectives

These are to:

1. test the feasibility and safety of customised 3D printed HPPD,

2. integrate the prostheses to the skull defect in removable manner and discharge patient with appropriate education,

3. to systematically monitor subjects for symptoms, compliance, complications and subjective feedback during the outpatient phase where progressive wear of HPPD and monitoring of acceptability will be monitored.

Conditions

Brain Injuries; Stroke

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Decompressive craniectomy

3D printed skull replacement piece will be fitted to subject.

Group Type: EXPERIMENTAL

Head protection prototype device

Intervention Type: DEVICE

The proposed experimental HPPD uses biocompatible material using FDMÔNylon which has high fatigue resistance, chemical resistance with impact resistance and toughness which is free of powders. It is HSA unclassified as yet and the FDMONylon is not FDA approved yet.

Interventions

Head protection prototype device

The proposed experimental HPPD uses biocompatible material using FDMÔNylon which has high fatigue resistance, chemical resistance with impact resistance and toughness which is free of powders. It is HSA unclassified as yet and the FDMONylon is not FDA approved yet.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Age 21 to 80 years, both males and females.

2. Presence of surgical unilateral or bilateral craniectomy performed for reasons of ischaemic or haemorrhagic stroke, Subarachnoid haemorrhage (SAH), traumatic brain injury (TBI), benign cerebral tumours, etc.

3. Stroke, SAH or TBI are diagnosed by specialists and confirmed on brain imaging studies (CT, MRI)

4. Duration from event > 30 days and either during inpatient or outpatient phase.

5. Presence of at least 1 post decompressive craniectomy CT brain film performed at NNI/TTSH.

6. Healed craniectomy surgical wound without bulging skin flap or active skin infection.

7. Patients awaiting elective cranioplasty or those who refuse cranioplasty. 8 Ability to understand simple instructions and give own consent. 9 Presence of family members or NOK who can supervise the patient to don the head protection device, care for the material and regularly monitor for compliance and complications 10 Reproductive age females should not be pregnant at the point of consent-taking and during the study

Exclusion Criteria

1. Patient in vegetative or minimally responsive state.

2. Presence of uncontrolled medical condition (uncontrolled hypertension, Diabetes Mellitus, sepsis or delirium, active malignancy either cranial or extracranial sites)

3. Presence of end organ failure (end stage renal or liver failure, renal dialysis, life expectancy <6 months)

4. Presence of pregnancy or lactation.

5. Presence of severe agitation /behavioural/active depression or anxiety/ drug or alcohol addiction which would negatively affect compliance,

6. Presence of unhealed head wound, active wound infection, scalp dermatitis, wound breakdown which would be worsened by pressure from the HPPD.

7. Presence of known allergy to the investigational products which is the 3D printed material (e.g. Nylon).

8. Subjects' CT brain imaging films are not available to the study team.

9. Absence of NOK who can assist monitoring unless subjects is able to self-monitor

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Creatz3D

UNKNOWN

Sponsor Role: collaborator

Tan Tock Seng Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Khai Pang Leong

Role: STUDY_DIRECTOR

Tan Tock Seng Hospital Clinical research and innovation office

Locations

Tan Tock Seng Hospital Rehabilitation Centre

Singapore, , Singapore

Countries

Singapore

Other Identifiers

DSRB2019/00155

Identifier Type: -

Identifier Source: org_study_id