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NOT YET RECRUITING
NCT07768605
NA

Clinical Evaluation of a Novel Textile Radiation Protection Device

Sponsor: Emory University

View on ClinicalTrials.gov

Summary

This study will use procedure-specific dosimetry to evaluate whether Texray's novel woven radiation protection fabric (HeadPeace and MindPeace) reduces occupational radiation dose to the head and thyroid of interventional radiology personnel compared with standard radiation protection equipment, and to explore variation in efficacy by role, procedure type, and fluoroscopy room/equipment characteristics.

Official title: Evaluation of Novel Woven Fabric Radiation Protection Gear for Head and Neck Regions for Interventional Radiology Personnel

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2026-08

Completion Date

2027-07

Last Updated

2026-08-17

Healthy Volunteers

No

Interventions

DEVICE

Standard PPE

Standard PPE (Baseline Phase): Participants wear their usual radiation protection equipment, including standard lead aprons and thyroid collars (and any head coverings they already use). Personal dosimeters are placed at predefined anatomical regions mimicking Texray coverage (e.g., forehead, temples, anterior/lateral thyroid) over standard PPE. These readings provide baseline scatter radiation exposure under current clinical conditions.

DEVICE

Texray PPE

Texray PPE (Intervention Phase): During the intervention phase, participants wear HeadPeace (non-lead head protector) and MindPeace (non-lead thyroid and face protector) during procedures. Each garment includes internal and external dosimeter pockets at key anatomical sites to enable paired measurements beneath and outside the shield. These data support calculation of percent dose reduction and attenuation at specific sites.

Locations (3)

Emory University Hospital Midtown

Atlanta, Georgia, United States

Winship Cancer Institute

Atlanta, Georgia, United States

Emory University Hospital

Atlanta, Georgia, United States